UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q
(Mark One)
x |
QUARTERLY REPORT PURSUANT TO SECTION 13 or 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934. |
For the quarterly period ended |
March 31, 2015 |
Commission file number 000-29449
POSITRON CORPORATION
(Exact Name of Registrant as specified in
its charter)
Texas |
|
76-0083622 |
(State or Other Jurisdiction of Incorporation or |
|
(IRS Employer Identification No.) |
Organization) |
|
|
530 Oakmont Lane, Westmont, Illinois |
|
60559 |
(Address of Principal Executive Offices) |
|
(Zip Code) |
Registrant’s Telephone Number, Including Area Code: (317)
576-0183
Indicate by check mark whether the issuer
(1) filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12
months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing
requirements for the past 90 days. Yes x No ¨
Indicate by check mark whether the registrant
has submitted electronically and posted on its corporate web site, if any, every Interactive Data File required to be submitted
and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter
period that the registrant was required to submit and post such files). Yes x No ¨
Indicate by check mark whether the registrant
is a larger accelerated filer, an accelerated filer, a non-accelerated or a smaller reporting company filer. See the definition
of “large accelerated filer, accelerated filer and smaller reporting company" in Rule 12b-2 of the Exchange Act. (Check
one)
Large accelerated filer ¨ |
Accelerated filer ¨ |
Non-accelerated filer ¨ |
Smaller reporting company x |
Indicate by check mark whether the registrant is a shell company
(as defined in Rule 12b-2 of the Exchange Act). Yes ¨
No x
The numbers of shares outstanding of common stock, par value
$0.0001 per share outstanding as of May 15, 2015: 14,275,797
POSITRON CORPORATION
TABLE OF CONTENTS
PART 1 – FINANCIAL INFORMATION
ITEM 1. Financial Statements
POSITRON CORPORATION AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
(In thousands, except share data)
| |
March 31, 2015 (Unaudited) | | |
December 31, 2014 | |
ASSETS | |
| | | |
| | |
| |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 79 | | |
$ | 208 | |
Accounts receivable, less allowance for doubtful accounts of $171 | |
| 164 | | |
| 175 | |
Inventories, less reserve of $513 | |
| 330 | | |
| 330 | |
Prepaid expenses | |
| 23 | | |
| 17 | |
Total current assets | |
| 596 | | |
| 730 | |
| |
| | | |
| | |
Property and equipment, less accumulated depreciation of $697 and $655 | |
| 879 | | |
| 919 | |
Intangible assets | |
| 9 | | |
| 9 | |
Other assets | |
| 201 | | |
| 211 | |
Total assets | |
$ | 1,685 | | |
$ | 1,869 | |
| |
| | | |
| | |
LIABILITIES AND STOCKHOLDERS’ DEFICIT | |
| | | |
| | |
| |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable, trade and accrued liabilities | |
$ | 807 | | |
$ | 849 | |
Unearned revenue | |
| 27 | | |
| 27 | |
Advances from related parties | |
| 564 | | |
| 600 | |
Notes payable – current portion | |
| 455 | | |
| 461 | |
Convertible debentures, less debt discount of $345 and $460 | |
| 115 | | |
| - | |
Embedded conversion derivative liabilities | |
| 662 | | |
| 760 | |
Total current liabilities | |
| 2,630 | | |
| 2,697 | |
| |
| | | |
| | |
Notes payable – noncurrent portion | |
| 8 | | |
| 9 | |
Total liabilities | |
| 2,638 | | |
| 2,706 | |
| |
| | | |
| | |
Stockholders’ deficit: | |
| | | |
| | |
Series A preferred stock: $1.00 par value; 8% cumulative, convertible, redeemable; 7,900,000 shares authorized; 447,652 shares issued and outstanding. | |
| 448 | | |
| 448 | |
Series B preferred stock: $1.00 par value; convertible, redeemable; 9,000,000 shares authorized; 249,985 and 262,485 shares issued and outstanding | |
| 249 | | |
| 262 | |
Common stock: $0.0001 par value; 9,000,000,000 shares authorized; 14,275,797 and 13,886,738 shares issued and outstanding | |
| 1 | | |
| 1 | |
Additional paid-in capital | |
| 124,934 | | |
| 124,483 | |
Accumulated deficit | |
| (126,570 | ) | |
| (126,016 | ) |
Treasury stock: 150 shares at cost | |
| (15 | ) | |
| (15 | ) |
Total stockholders’ deficit | |
| (953 | ) | |
| (837 | ) |
Total liabilities and stockholders’ deficit | |
$ | 1,685 | | |
$ | 1,869 | |
See accompanying notes to consolidated financial
statements
POSITRON CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS
OF OPERATIONS
(In thousands, except per share data)
(Unaudited)
| |
For The Three Months Ended | |
| |
March 31, 2015 | | |
March 31, 2014 | |
| |
| | |
| |
Sales: | |
$ | 346 | | |
$ | 456 | |
| |
| | | |
| | |
Costs of sales: | |
| 210 | | |
| 428 | |
| |
| | | |
| | |
Gross profit | |
| 136 | | |
| 28 | |
| |
| | | |
| | |
Operating expenses: | |
| | | |
| | |
General and administrative | |
| 505 | | |
| 565 | |
Research and development | |
| 120 | | |
| 102 | |
Selling and marketing | |
| 42 | | |
| 46 | |
| |
| | | |
| | |
Total operating expenses | |
| 667 | | |
| 713 | |
| |
| | | |
| | |
Loss from operations | |
| (531 | ) | |
| (685 | ) |
| |
| | | |
| | |
Other income (expense) | |
| | | |
| | |
Interest expense | |
| (136 | ) | |
| (396 | ) |
Derivative gain | |
| 98 | | |
| 220 | |
Other | |
| 15 | | |
| - | |
| |
| | | |
| | |
Total other income (expense) | |
| (23 | ) | |
| (176 | ) |
| |
| | | |
| | |
Loss before income taxes | |
| (554 | ) | |
| (861 | ) |
| |
| | | |
| | |
Income taxes | |
| - | | |
| - | |
| |
| | | |
| | |
Net loss | |
$ | (554 | ) | |
$ | (861 | ) |
| |
| | | |
| | |
Basic and diluted loss per common share | |
$ | (0.04 | ) | |
$ | (0.24 | ) |
| |
| | | |
| | |
Basic and diluted weighted average shares outstanding | |
| 14,060 | | |
| 3,631 | |
See accompanying notes to consolidated financial
statements
POSITRON CORPORATION AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
(In thousands)
(Unaudited)
| |
Three Months Ended | |
| |
March 31, 2015 | | |
March 31, 2014 | |
Cash flows from operating activities: | |
| | | |
| | |
Net loss | |
$ | (554 | ) | |
$ | (861 | ) |
Adjustment to reconcile net loss to net cash used in operating activities | |
| | | |
| | |
Depreciation and amortization | |
| 40 | | |
| 36 | |
Stock based compensation | |
| 159 | | |
| - | |
Derivative gain | |
| (98 | ) | |
| (220 | ) |
Common stock issued for services | |
| 29 | | |
| - | |
Accretion of debt discount | |
| 115 | | |
| 381 | |
Changes in operating assets and liabilities: | |
| | | |
| | |
Accounts receivable | |
| 11 | | |
| (1 | ) |
Inventories | |
| - | | |
| (77 | ) |
Prepaid expenses and other assets | |
| 4 | | |
| - | |
Accounts payable, trade and accrued liabilities | |
| (42 | ) | |
| (86 | ) |
Unearned revenue | |
| - | | |
| (21 | ) |
| |
| | | |
| | |
Net cash used in operating activities | |
| (336 | ) | |
| (695 | ) |
| |
| | | |
| | |
Cash flows from investing activities: | |
| | | |
| | |
Purchase of property and equipment | |
| - | | |
| (2 | ) |
| |
| | | |
| | |
Net cash used in investing activities | |
| - | | |
| (2 | ) |
| |
| | | |
| | |
Cash flows from financing activities: | |
| | | |
| | |
Payments on note payable | |
| (7 | ) | |
| (24 | ) |
Payment of noninterest bearing advances | |
| (36 | ) | |
| (165 | ) |
Proceeds from convertible debt | |
| - | | |
| 320 | |
Proceeds from issuance of common stock | |
| 250 | | |
| - | |
| |
| | | |
| | |
Net cash provided by financing activities | |
| 207 | | |
| 131 | |
| |
| | | |
| | |
Net decrease in cash and cash equivalents | |
| (129 | ) | |
| (566 | ) |
| |
| | | |
| | |
Cash and cash equivalents, beginning of period | |
| 208 | | |
| 1,744 | |
| |
| | | |
| | |
Cash and cash equivalents, end of period | |
$ | 79 | | |
$ | 1,178 | |
| |
| | | |
| | |
Supplemental cash flow information: | |
| | | |
| | |
Interest paid | |
$ | 14 | | |
$ | 8 | |
| |
| | | |
| | |
Income taxes paid | |
$ | - | | |
$ | - | |
| |
| | | |
| | |
Non-cash disclosures: | |
| | | |
| | |
Conversion of convertible debenture, accrued interest and derivative liability to common stock payable | |
$ | - | | |
$ | 6,893 | |
| |
| | | |
| | |
Conversion of Series B Preferred Stock to Common Stock | |
$ | 13 | | |
$ | - | |
See accompanying notes to consolidated financial
statements
POSITRON CORPORATION AND SUBSIDIARIES
SELECTED NOTES TO CONSOLIDATED FINANCIAL
STATEMENTS
(Unaudited)
The accompanying unaudited interim
financial statements have been prepared in accordance with generally accepted accounting principles and the rules of the U.S. Securities
and Exchange Commission, and should be read in conjunction with the audited financial statements and notes thereto contained in
the Annual Report on Form 10-K for Positron Corporation (the “Registrant” or the “Company”) for the year
ended December 31, 2014. In the opinion of management, all adjustments, consisting of normal recurring adjustments, necessary for
a fair presentation of financial position, results of operations and cash flows for the interim periods presented have been reflected
herein. The results of operations for interim periods are not necessarily indicative of the results to be expected for the full
year. Notes to the financial statements which would substantially duplicate the disclosures contained in the audited financial
statements for the most recent fiscal year ended December 31, 2014, as reported in the Form 10-K, have been omitted.
In preparing the interim unaudited
consolidated financial statements, management was required to make certain estimates and assumptions that affect the reported amounts
of assets, liabilities, revenues, expenses and related disclosures at the financial reporting date and throughout the periods being
reported upon. Certain of the estimates result from judgments that can be subjective and complex and consequently actual results
may differ from these estimates.
All significant intercompany
balances and transactions have been eliminated.
For a summary of significant
accounting policies (which have not changed from December 31, 2014), see the Company’s Annual Report on Form 10-K for the
year ended December 31, 2014.
Use of Estimates
The preparation of financial
statements in conformity with accounting principles generally accepted in the United States requires management to make estimates
and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities
at the date of the financial statements as well as the reported amount of revenues and expenses during the reporting period. Actual
results could differ from these estimates.
Intangible Assets
The Company also reviews its
identified intangible assets for impairment whenever events or circumstances indicate that the carrying amount of an asset may
not be recoverable. The Company assesses recoverability by reference to future cash flows from the products underlying these intangible
assets. If these estimates change in the future, the Company may be required to record impairment charges for these assets. As
of March 31, 2015, no impairment was recorded.
Debt Discount
Costs incurred with parties who
are providing long-term financing, which generally include the value of warrants or the fair value of an embedded derivative conversion
feature, are reflected as a debt discount and are amortized over the life of the related debt. The Company recorded the accretion
of debt discount of $115,000 and $381,000 during the three months ended March 31, 2015 and 2014, respectively. The total unaccreted
debt discount at March 31, 2015 was $345,000, compared to $460,000 at December 31, 2014.
Fair Value of Financial
Instruments
The carrying value of cash and
cash equivalents, accounts receivable, prepaids, deposits, accounts payable and accrued liabilities, common stock payable, and
unearned revenue, approximate their fair values because of the short-term nature of these instruments. Management believes
the Company is not exposed to significant interest or credit risks arising from these financial instruments.
Fair value is defined as the
exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous
market for the asset or liability in an orderly transaction between market participants on the measurement date. Valuation techniques
used to measure fair value maximize the use of observable inputs and minimize the use of unobservable inputs. The Company utilizes
a fair value hierarchy based on three levels of inputs, of which the first two are considered observable and the last unobservable.
| • | Level 1 — Quoted prices in active markets for identical assets or liabilities. These are
typically obtained from real-time quotes for transactions in active exchange markets involving identical assets. |
| • | Level 2 — Quoted prices for similar assets and liabilities in active markets; quoted prices
included for identical or similar assets and liabilities that are not active; and model-derived valuations in which all significant
inputs and significant value drivers are observable in active markets. These are typically obtained from readily-available pricing
sources for comparable instruments. |
| • | Level 3 — Unobservable inputs, where there is little or no market activity for the asset
or liability. These inputs reflect the reporting entity’s own beliefs about the assumptions that market participants would
use in pricing the asset or liability, based on the best information available in the circumstances. |
The following table presents
the embedded conversion derivative liability, the Company’s only financial liability measured and recorded at fair value
on the Company’s consolidated balance sheets on a recurring basis and their level within the fair value hierarchy as of March
31, 2015 (in thousands):
| |
March 31, 2015 | | |
Level 1 | | |
Level 2 | | |
Level 3 | |
| |
| | | |
| | | |
| | | |
| | |
Embedded conversion derivative liability | |
$ | 662 | | |
$ | - | | |
$ | - | | |
$ | 662 | |
The following table reconciles,
for the three months ended March 31, 2015, the beginning and ending balances for financial instruments that are recognized at fair
value in the consolidated financial statements (in thousands):
Balance of embedded conversion derivative liability as of December 31, 2014 | |
$ | 760 | |
Gain on fair value adjustments to embedded conversion derivative liability | |
| (98 | ) |
Balance of embedded conversion derivative liability at March 31, 2015 | |
$ | 662 | |
The fair value of the conversion
features are calculated at the time of issuance and the Company records a derivative liability for the calculated value using a
Black-Scholes option-pricing model. Changes in the fair value of the derivative liability are recorded in other income (expense)
in the consolidated statements of operations. Upon conversion of the convertible debt to stock, the Company reclassifies the related
embedded conversion derivative liability to paid in capital. Since the fair value of the embedded conversion derivative liability
exceeded the carrying value of the convertible debentures on the issuance date, the convertible debentures were recorded at a full
discount. The Company recognizes expense for accretion of the convertible debentures discount over the term of the notes. The Company
has considered the provisions of ASC 480, Distinguishing Liabilities from Equity, as the conversion feature embedded in
each debenture could result in the note principal being converted to a variable number of the Company’s common shares.
Revenue Recognition
The Company’s revenues
are currently derived from the sale of medical equipment products, maintenance contracts and service revenues. Revenues from maintenance
contracts are recognized over the term of the contract. Service revenues are recognized upon performance of the services. The Company
recognizes revenues from the sale of medical equipment products when earned. Specifically, revenue is recognized when persuasive
evidence of an arrangement exists, delivery has occurred (or services have been rendered), the price is fixed or determinable,
and collectability is reasonably assured. The Company obtains a signed customer acceptance after installation is complete for the
sale of its Attrius® systems.
In multiple-element arrangements,
revenue is allocated to each element based on their relative selling prices. Relative selling prices are based first on vendor
specific objective evidence (VSOE), then on third-party evidence of selling price (TPE) when VSOE does not exist, and then on estimated
selling price (ESP) when VSOE and TPE do not exist. Because the Company has neither VSOE nor TPE for its products, the allocation
of revenue has been based on the Company’s ESPs. The objective of ESP is to determine the price at which the Company would
transact a sale if the product was sold on a stand-alone basis. The Company determines ESP by considering the facts and circumstances
of the product being sold.
Recent Accounting Pronouncements
In May 2014, the FASB issued
Accounting Standards Update No. 2014-09, Revenue from Contracts with Customers (ASU 2014-09), which supersedes nearly all existing
revenue recognition guidance under U.S. GAAP. The core principle of ASU 2014-09 is to recognize revenues when promised goods or
services are transferred to customers in an amount that reflects the consideration to which an entity expects to be entitled for
those goods or services. ASU 2014-09 defines a five step process to achieve this core principle and, in doing so, more judgment
and estimates may be required within the revenue recognition process than are required under existing U.S. GAAP.
The standard is effective for
annual periods beginning after December 15, 2017, and interim periods therein, using either of the following transition methods:
(i) a full retrospective approach reflecting the application of the standard in each prior reporting period with the option to
elect certain practical expedients, or (ii) a retrospective approach with the cumulative effect of initially adopting ASU 2014-09
recognized at the date of adoption (which includes additional footnote disclosures). We are currently evaluating the impact of
our pending adoption of ASU 2014-09 on our consolidated financial statements and have not yet determined the method by which we
will adopt the standard in 2018.
On May 8, 2014, our Board of
Directors and shareholders holding more than two-thirds of the Company’s voting stock approved a reverse split of the Company’s
Common Stock on a 1 for 400 basis (the, “Reverse Split”). The Company filed a Definitive Information Statement with
the Securities and Exchange Commission on November 18, 2014 to effectuate the Reverse Split.
On April 8, 2015, the
effective date of the Reverse Stock Split, every 400 shares of the Company’s issued and outstanding common stock were
combined into one share of common stock. The Company did not issue any fractional shares in connection with the reverse stock
split. Stockholders of record who otherwise would have been entitled to receive fractional shares were entitled, to one
share.
Throughout this report, each
instance which refers to a number of shares of our common stock refers to the number of shares of common stock after giving effect
to the Reverse Split, unless otherwise indicated. References to a number of shares of common stock in our historical
financial statements for the year ended December 31, 2014 are reported on a post-Reverse Split basis.
Since its inception, the Company
has expended substantial resources on research and development and sustained losses. Due to the limited number of systems sold
or placed into service each year, revenues have fluctuated significantly from year to year and have not been sufficient to be operationally
profitable. The Company had an accumulated deficit of $126,570,000 and a stockholders’ deficit of $953,000 at March 31, 2015.
The Company will need to increase sales and apply the research and development advancements to achieve profitability in the future.
The Company will need to resume and increase sales of PET and radiopharmaceutical systems, services, radiopharmaceuticals and radioisotope
sales and apply the research and development advancements to achieve profitability in the future. There can be no assurance that
the Company will continue to be successful in selling products.
The Company had cash and cash
equivalents of $79,000 at March 31, 2015. At the same date, the Company had accounts payable and accrued liabilities of $807,000
and a negative working capital of $2,034,000. Working capital requirements for the upcoming year will reach beyond our current
cash balances. The Company plans to continue to raise funds as required through equity and debt financing to sustain business operations.
These factors raise substantial doubt about the Company’s ability to continue as a going concern.
There can be no assurance that
the Company will be successful in implementing its business plan and ultimately achieving operational profitability. The Company’s
long-term viability as a going concern is dependent on its ability to 1) achieve adequate profitability and cash flows from operations
to sustain its operations, 2) control costs and expand revenues from existing or new business 3) meet current commitments and fund
the continuation of its business operation in the near future and 4) raise additional funds through debt and/or equity financings.
Other assets at March 31, 2015
and December 31, 2014 consisted of $201,000 in deposits paid to our joint venture partner, Neusoft for Attrius® systems.
Inventories at March 31, 2015
and December 31, 2014 consisted of the following (in thousands):
| |
March 31, 2015 | | |
December 31, 2014 | |
Finished systems | |
$ | - | | |
$ | - | |
Raw materials and service parts | |
| 422 | | |
| 422 | |
Work in progress | |
| 421 | | |
| 421 | |
| |
| 843 | | |
| 843 | |
Less: Reserve for obsolete inventory | |
| (513 | ) | |
| (513 | ) |
| |
$ | 330 | | |
$ | 330 | |
Inventories are stated at the
lower of cost or market. Cost is determined using the first-in, first-out (FIFO) method of inventory valuation. The
Company evaluated the reserve as of March 31, 2015 and December 31, 2014.
Property and equipment at March
31, 2015 and December 31, 2014 consisted of the following (in thousands):
| |
March 31, 2015 | | |
December 31, 2014 | |
Buildings | |
$ | 500 | | |
$ | 500 | |
Furniture and fixtures | |
| 88 | | |
| 88 | |
Leasehold improvements | |
| 72 | | |
| 72 | |
Computer equipment | |
| 76 | | |
| 76 | |
Research equipment | |
| 679 | | |
| 679 | |
Machinery and equipment | |
| 158 | | |
| 158 | |
| |
| 1,573 | | |
| 1,573 | |
Less: Accumulated depreciation | |
| (694 | ) | |
| (654 | ) |
| |
$ | 879 | | |
$ | 919 | |
8. |
Accounts Payable and Accrued Liabilities |
Accounts payable and accrued liabilities at March
31, 2015 and December 31, 2014 consisted of the following (in thousands):
| |
March 31, 2015 | | |
December 31, 2014 | |
Trade accounts payable | |
$ | 598 | | |
$ | 660 | |
Accrued interest | |
| 69 | | |
| 59 | |
Sales taxes payable | |
| 73 | | |
| 79 | |
Accrued compensation | |
| 47 | | |
| 47 | |
Other accrued expenses | |
| 20 | | |
| 4 | |
| |
| | | |
| | |
Total | |
$ | 807 | | |
$ | 849 | |
Basic loss per common share is
based on the weighted average number of common shares outstanding in each period and earnings adjusted for preferred stock dividend
requirements. Diluted earnings per common share assumes that any dilutive convertible preferred shares outstanding at the beginning
of each period were converted at those dates, with related interest, preferred stock dividend requirements and outstanding common
shares adjusted accordingly. It also assumes that outstanding common shares were increased by shares issuable upon exercise of
those stock options and warrants for which market price exceeds exercise price, less shares which could have been purchased by
the Company with related proceeds. The convertible preferred stock and outstanding stock options and warrants were not included
in the computation of diluted earnings per common share for the three months ended March 31, 2015 and 2014, respectively since
it would have resulted in an antidilutive effect.
The following table sets forth
the computation of basic and diluted loss per share (in thousands, except per share data):
| |
Three Months Ended | |
| |
March 31, 2015 | | |
March 31, 2014 | |
| |
| |
Numerator | |
| | | |
| | |
Basic and diluted loss | |
$ | (554 | ) | |
$ | (861 | ) |
| |
| | | |
| | |
Denominator | |
| | | |
| | |
Basic and diluted earnings per share - weighted average shares outstanding | |
| 14,060 | | |
| 3,631 | |
| |
| | | |
| | |
Basic and diluted loss per common share | |
$ | (0.04 | ) | |
$ | (0.24 | ) |
Anti-dilutive securities (based
on conversions to common shares) not included in net loss per share calculation (in thousands):
| |
March 31, 2015 | | |
March 31, 2014 | |
Convertible Series A preferred stock | |
| 1 | | |
| 1 | |
Convertible Series B preferred stock | |
| 62 | | |
| 764 | |
Convertible Series S preferred stock | |
| - | | |
| 2,500 | |
Convertible Series H preferred stock | |
| - | | |
| 1,207 | |
Stock warrants | |
| 33 | | |
| 306 | |
Convertible debt | |
| 4 | | |
| 1,009 | |
Common stock options | |
| 269 | | |
| 472 | |
Series B preferred stock options | |
| 343 | | |
| 516 | |
Common stock payable | |
| - | | |
| 3,446 | |
| 10. | Convertible Debentures |
During the three months ending
March 31, 2015, the Company issued no convertible debentures.
During the three months ended
March 31, 2015 and 2014, the Company recognized $115,000 and $381,000, respectively, of interest expense on the Convertible Debentures.
| |
March 31, 2015 | |
| |
| |
Convertible debentures | |
$ | 460 | |
Debt discount | |
| (345 | ) |
Net convertible debentures | |
$ | 115 | |
| 11. | Notes Payable and advances from related parties |
On January 17, 2012, the Company
assumed from MIT a note payable with Los Alamos National Bank (“LANB”) in the amount of $700,000. On February 10, 2012,
MIT refinanced with LANB the principal and accrued interest of this note payable with a promissory note of $708,000, maturing on
February 10, 2015. The monthly payment to LANB on the promissory note is $11,105 and a balloon payment of $453,433 due in February
2015, with the interest rate of 10.0% at March 31, 2015. The promissory note is guaranteed by the Company and secured by all assets
of the Company. Total interest paid on the promissory note was $14,000 during the three months ended March 31, 2015. The note’s
outstanding amount was $451,000 at March 31, 2014. The Company is currently in default on the note with LANB and has received a
demand letter for the unpaid principal and interest.
As of March 31, 2015, the
Company had outstanding advances of $600,000. These advances are short term notes from their CFO and former CEO to help
fund operations. The notes are unsecured and non-interest bearing.
The Company has entered into
a capital lease for equipment at interest rates of 7.25%, payable through 2018. The asset and liability under the capital lease
is recorded at the present value of the minimum lease payments and are depreciated over their estimated useful lives. The gross
amount of assets held under capital leases for the three months ended March 31, 2015 and year ended December 31, 2014 was $16,300,
respectively, with accumulated depreciation of $4,075 and $2,300, respectively. Depreciation expense for this equipment for the
three months ended March 31, 2015 and 2014 was $1,775 and $1,135, respectively.
Future maturities of notes payable,
advances and capital leases are as follows:
March 31, | |
| | |
2015 | |
$ | 1,019,000 | |
2016 | |
| 4,000 | |
2017 | |
| 3,000 | |
2018 | |
| 1,000 | |
Total | |
| 1,027,000 | |
Less: current portion | |
| (1,019,000 | ) |
Note payable – noncurrent portion | |
$ | 8,000 | |
2015
Effective April 8, 2015 (see Note 3), the
Company effected a 1-for-400 reverse stock split.
In February 2015, the Company
issued an aggregate of 387,848 shares of Common Stock. 37,500 shares were issued for consulting services performed. The
Common Stock had a fair market value of $0.0019 per share and the Company recorded $28,500 for consulting services. The Company
also issued an aggregate of 3,125 shares from the conversion of 12,500 shares of the Company’s Series B Convertible Preferred
Stock into Common Stock, and sold 347,223 shares for $250,000.
2014
As of March 31, 2014, the Company had common stock
payable of $6,893,000. Various holders of convertible debt submitted their debt for conversion but the shares were not available
for issuance due to the lack of authorized shares.
For all of the Company’s
stock-based compensation plans, the fair value of each grant was estimated at the date of grant using the Black-Scholes option-pricing
model. Black-Scholes utilizes assumptions related to volatility, the risk-free interest rate, the dividend yield (which is assumed
to be zero, as the Company has not paid cash dividends to date and does not currently expect to pay cash dividends) and the expected
term of the option. Expected volatilities utilized in the model are based mainly on the historical volatility of the Company’s
stock price over a period commensurate with the expected life of the share option as well as other factors. The risk-free interest
rate is derived from the zero-coupon U.S. government issues with a remaining term equal to the expected life at the time of grant.
For options issued during 2012,
fifty percent (50%) of the options vested immediately on the grant date with the remaining fifty percent (50%) vesting on January
17, 2013. The company recognized compensation expense of $88,000 during the first quarter of 2013.
In 2015, the Board extended the
outstanding options to January 17, 2020. The options vest immediately and company recognized compensation expense of $159,000 during
the first quarter of 2015.
Fair market value using the
Black-Scholes option-pricing model was determined using the following assumptions:
Expected life (years) | |
5 |
Risk free rate of return | |
1.29% |
Dividend yield | |
0 |
Expected volatility | |
193% |
| 14. | Related Party Transactions |
2015
During the period January 1,
2015 through March 31, 2015, the Company repaid $36,250 to its former CEO from related advances.
2014
During the period January 1,
2014 through March 31, 2014, the Company repaid $57,500 to its former CEO from related advances.
During the period January 1,
2014 through March 31, 2014, the Company repaid $107,500 to its CFO from related advances.
During the period January 1,
2014 through March 31, 2014, the Company paid consulting fees in the amount of $37,000 to the brother of its then CEO.
Lease Agreements
On March 30, 2015, the Company
entered into an agreement to terminate an operating lease with a third party for space in Fishers, Indiana. The Company is required to pay termination fees of $25,865 to the lessor. At March 31, 2015
there were accrued termination fees of $15,670 net of the security deposit.
On April 19, 2010, the Company entered into an operating
lease agreement with a third party for warehousing and office space in Niagara, New York. The lease expires in May 2016, with an
option to renew for an additional three years. Monthly rent is $1,600.
On December 5, 2011, MIT entered
into an operating lease with a third party for space for warehousing at a building in Lubbock, Texas. The Company will be required
to make payments of $1,475 each month from month to month.
Litigation
On June 8, 2012, the owner of
the radiopharmaceutical manufacturing facility the Company formerly leased in Crown Point, Indiana commenced an action to recover
the use of the premises and the remaining rent due under the lease. On November 14, 2012, the owner was awarded a judgment against
the Company in the amount of $85,525.98 plus interest at the rate of 8%. The Company and the owner agreed to monthly payments in
the minimum amount of $5,000 until the judgment is paid in its entirety. Upon determination of the disposition of the Company’s
security deposit, the terms of the judgment will be completed.
In May, 2013, the Company was
served with a First Amended Complaint in action commenced against its former CEO and principal shareholder. The plaintiff in the
action is seeking to enforce a judgment against the former CEO and principal shareholder and is seeking to have the Company’s
Westmont, Illinois offices, which it purchased from the former CEO, reconveyed. The related party defendants have disputed the
basis of the judgment and the Company has denied the allegations in the Complaint and is defending the action. The Plaintiff recently
filed a motion to amend its complaint to seek the return of $1,917,000 of the funds invested by Solaris, plus interest, from the
Company. The motion has not yet been heard by the court.
On October 8, 2014, the Company
accepted service of a Summons and Complaint in an action commenced by the Securities and Exchange Commission (the “Commission),
in the United States District Court for the Southern District of Florida. The complaint alleges the Company’s former
Chairman, CEO and principal stockholder and the Company engaged in fraudulent activity to manipulate the Company’s stock.
The complaint alleges that the former CEO was involved in compensating a confidential informant, who was a former consultant to
the Company, $1,000 to encourage interest and buying in the Company’s stock. The Commission's complaint alleges that the
defendants violated Section 10(b) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”) and Rules
10b-5(a) and 10b-5(c). The Commission is seeking injunctions from future violations and civil money penalties against the Company.
Without admitting or denying the allegations in the complaint, the Company entered into a settlement with the Commission and agreed
not to violate Section 10(b) and Rule 10b-5(a) and (c) of the Exchange Act and to have the determination of any monetary penalty
be decided in a judicial hearing, which has not yet been scheduled.
We have aggregated our operations
into two reportable segments based upon product lines, manufacturing processes, marketing and management of our businesses: medical
equipment and radiopharmaceuticals. Our business segments operate in the nuclear medicine industry. The Company’s
medical equipment segment is currently generating all revenues and the majority of all expenses as the radiopharmaceuticals segment
awaits the availability of additional radioisotopes from manufacturers.
We evaluate a segment’s
performance based primarily upon operating income before corporate expenses.
Corporate assets consist primarily
of cash but also include plant and equipment associated with our headquarters. These items (and income and expenses related
to these items) are not allocated to the segments. Unallocated income/expenses include interest income, interest expense, debt
extinguishment and refinancing costs and other (expense) income and certain expenses which are not considered related to either
segment, but are instead considered general corporate expenses.
The following table represents
sales, operating loss and total assets attributable to these business segments for the periods indicated (in thousands):
| |
Three Months Ended | |
| |
March 31, 2015 | | |
March 31, 2014 | |
Total Sales: | |
| | | |
| | |
Medical equipment | |
$ | 346 | | |
$ | 456 | |
Radiopharmaceuticals | |
| - | | |
| - | |
Total sales | |
$ | 346 | | |
$ | 371 | |
| |
| | | |
| | |
Operating Loss: | |
| | | |
| | |
Medical equipment | |
$ | (384 | ) | |
$ | (482 | ) |
Radiopharmaceuticals | |
| (147 | ) | |
| (203 | ) |
Unallocated | |
| - | | |
| - | |
Total operating loss | |
$ | (531 | ) | |
$ | (685 | ) |
| |
| | | |
| | |
Total Assets: | |
| | | |
| | |
Medical equipment | |
$ | 1,289 | | |
$ | 2,722 | |
Radiopharmaceuticals | |
| 396 | | |
| 484 | |
Unallocated | |
| - | | |
| - | |
Total assets | |
$ | 1,685 | | |
$ | 3,206 | |
ITEM 2 - MANAGEMENT’S DISCUSSION AND ANALYSIS OF FINANCIAL
CONDITION AND RESULTS OF OPERATIONS
The Company is including the
following cautionary statement in this Quarterly Report on Form 10-Q to make applicable and utilize the safe harbor provision of
the Private Securities Litigation Reform Act of 1995 regarding any forward-looking statements made by, or on behalf of, the Company.
Forward-looking statements include statements concerning plans, objectives, goals, strategies, future events or performance and
underlying assumptions and other statements, which are other than statements of historical facts. Certain statements contained
herein are forward-looking statements and, accordingly, involve risks and uncertainties, which could cause actual results or outcomes
to differ materially from those expressed in the forward-looking statements.
The Company’s expectations,
beliefs and projections are expressed in good faith and are believed by the Company to have a reasonable basis, including without
limitations, examination of historical operating trends, data contained in records and other data available from third parties,
but there can be no assurance that the Company’s expectations, beliefs or projections will result, or be achieved, or be
accomplished.
Overview
Positron is a nuclear medicine healthcare
company specializing in the business of cardiac Positron Emission Tomography (PET). Cardiac PET is the superior method in diagnostic
nuclear imaging for the detection of coronary artery disease (CAD), a leading cause of death in the United States. Positron’s
products and services empower healthcare providers to more accurately diagnose CAD and improve patient outcomes while practicing
cost effective medicine.
Positron is working
on providing an economical, end-to-end solution for PET myocardial perfusion imaging through complementary product integration
of PET imaging systems, radiopharmaceuticals, and radioisotopes.
Positron's goal
is to gain a dominant market position with strong earnings potential, ultimately becoming a sustained, long-term value creator
for industry participants and our shareholders.
The Company
Positron, a pioneer
in nuclear cardiology for over 30 years, is establishing a unique position in the cardiac PET marketplace by
vertically integrating the fragmented and limited supply environment that exists today. Positron’s approach is to
provide nuclear cardiologists an end-to-end solution by offering award-winning imaging technology, clinical services, imaging
agents and innovative financing packages conveniently from a single source. Securing the cardiac PET supply chain will
help to accelerate the adoption of this superior modality and growth of the nuclear
cardiology industry.
An important factor for
the growth of cardiac PET is the increase the supply of Strontium-82 (Sr-82), parent isotope of the most widely used cardiac
imaging agent Rubidium-82 (Rb-82). Constrained manufacturing capacity of Rubidium-82 generators and limited Sr-82 supply
are the primary reason for stagnant growth of cardiac PET despite demand potentially being at an all-time high.
Industry demand and supply limitations have created significant opportunities in Positron’s pursuit to
aggregate and integrate each critical component in the cardiac PET imaging value chain.
Positron is focused on increasing Sr-82
supply through radioisotope processing and production. Positron has supply agreements and technology partnerships with global irradiators
that produce Sr-82. Positron believes to be the only company in the U.S. that possesses the expertise, technical resources,
FDA acceptance and strategic relationships to have an immediate impact on the Sr-82 supply. Through multiple radioactive material
sources, including potentially the Company’s own high-energy cyclotron dedicated to the production of Sr-82, Positron intends
to introduce additional supply of Sr-82 into the marketplace, leading to an increase in the availability of Rb-82 generators and
the need for PET systems.
Positron believes PET is the future of
nuclear cardiology and Positron’s ability to offer the award-winning nuclear imaging technology and clinical services supplemented
by the supply of key radioisotopes positions Positron as the industry’s authority in the business of cardiac PET.
Positron intends
to maximize market share by offering cost-effective, value added solutions to end-users that meet the current and future nuclear
cardiology market demands.
PET vs. SPECT
There
are two main imaging modalities utilized in nuclear cardiology: Single Photon Emission Computed Tomography, or SPECT, and Positron
Emission Tomography, or PET.
In
myocardial perfusion imaging, PET has been proven to be superior in sensitivity and specificity when compared to SPECT, the more
commonly utilized modality. Cardiac PET scans, with Rb-82 Chloride or Nitrogen-13 Ammonia (N-13), result in a lower patient radiation
exposure and capable of performing superior quantitative measurements such as coronary flow reserve. Cardiac PET imaging has been
shown to provide a 50% reduction in invasive coronary arteriography and coronary artery bypass grafting, leading to a 30% costs
savings and improved clinical outcomes, when compared to SPECT (M.E. Merhige, M.D., et al. Journal Nuclear Medicine 2007; 48:1069-1076).
The
cardiac PET equipment market is much smaller than SPECT, but has seen significant annual growth of 30% during the last decade.
Based on Company estimates there were approximately 170 dedicated cardiac PET & PET/CT scanners performing nuclear cardiology
within the U.S. in 2014, a tenfold increase since 2006.
Barriers
to entry
For
many years, one of the major constraints for adoption of this modality had been the high cost of PET and PET/CT scanners. Many
practices and hospitals could not justify the cost of a new system for cardiac studies. In 2009, Positron received FDA clearance
to market and distribute its dedicated PET system, which is optimized for nuclear cardiology. The Attrius is the only new, cost
effective, dedicated PET system available on the market. Other system manufacturers (GE, Philips, Siemens) offer PET/CT cameras,
which have a 200%-300% higher purchase price; PET/CT systems also possess attributes that may affect the accuracy of a perfusion
study, leading to false positives.
Another
more recent issue that has slowed the growth of nuclear cardiology is the shortage of the key drugs utilized in both SPECT (Mo-99/Tc-99m)
and PET imaging (Sr-82/Rb-82).
The
Sr-82 isotope decays to produce the Rb-82 tracer utilized in cardiac PET studies. Rb-82 is the most commonly used cardiac PET tracer
in the United States. The FDA approved Rb-82 in 1989 for use in the detection of coronary artery disease and the Health Care Financing
Administration approved reimbursement for Rb-82, PET MPI, in 1995 as a first line test in symptomatic patients. Rubidium is uniformly
available through generator production in the U.S. and is used in conjunction with an automatic infusion system.
The
explosive growth of cardiac PET imaging from 2001-2011 has driven a significant increase in the use of Sr-82/Rb-82 generators.
The demand for Sr-82 is beginning to outpace supply. Due to the growing demand and limited supply, the industry suffered a Sr-82
shortage in January 2011, effecting the supply of Rb-82 generators. The same year Bracco Diagnostics Inc., the sole market supplier
of the Rb-82 generator, underwent a voluntary recall of generators, further stunting industry sales and growth. Though delivery
of Bracco's generators to existing clients was restored in 2013, the supply is essentially flat due to a combination of limited
generator manufacturing capabilities and limited availability of additional Sr-82.
Positron
is acutely focused on additional supply of Sr-82. Until recently, the U.S. Department of Energy had been the only entity in the
United States capable of producing this material. In August of 2012, Positron's whole-owned subsidiary, MIT, registered its DMF
with the FDA and has begun limited production of API grade strontium-82 from foreign irradiated targets.
To
address the long term solution of supply, Positron continues its pursuit of building a high-energy cyclotron dedicated to Sr-82
production. The U.S. cardiac PET market can support several high-energy cyclotrons. Positron's technological leadership in Sr-82
production and processing provides us with a significant advantage over other companies seeking to deliver Sr-82.
Positron
anticipates the cardiac PET market to rebound in Q4 2015, beginning with Bracco’s ability to now accept new generator customers,
and with accelerated expansion upon market entry of the DraxImage’s generator, once FDA approved.
Our
Market
According
to the U.S. Department of Health and Human Services, there are more than 22,000 cardiovascular diseases specialists in the U.S.,
and their number will increase to 31,000 by 2020. This is the target market for our products and services, as well as hospitals
in the United States that performs or could perform nuclear cardiac procedures and want to automate the delivery of radiopharmaceuticals.
By adding complimentary products, we will be able to offer customers value added solutions which include low cost molecular imaging
devices, maintenance service, disease specific software, radiopharmaceutical unit doses drawing devices, and, potentially, radiopharmaceuticals
agents for Cardiac Nuclear Medicine.
Cardiac
Nuclear Medicine helps in the diagnosis, management and prevention of cardiovascular disease (CVD) in patients. Radiopharmaceuticals
are injected into a patient to provide the most accurate, non-invasive test for identifying narrowed coronary arteries, mild cholesterol
build-up or diffuse coronary vascular disease, conditions that are responsible for almost all heart attacks.
Cardiovascular
disease is the leading cause of death in the United States and constitutes 17% of overall national health expenditures (Forecasting
the Future of Cardiovascular Disease in the United States, American Heart Association, 2011). Direct CVD costs are projected to
increase from $273 Billion, in 2010, to $818 Billion, in 2030; with indirect costs, due to lost productivity, expected to rise
from $172 Billion to $276 Billion by 2030.
Market
Potential
Although,
since 2011, the cardiac PET industry has experienced its most challenging years ever, the Company has been able to aggressively
pursue its strategy of aggregating and integrating the key components critical in securing the cardiac imaging supply chain. Positron
is dedicated to lowering the barriers that have been constricting, or could later constrict, the progress of medical advancements
in cardiac PET. Through our efforts to supplement the supply of key radioisotopes and our ability to offer innovative products
and services, management has methodically positioned Positron to become the industry’s only end-to-end solutions provider.
We
believe that Positron is the only company with the critical components to vertically integrate the fragmented “single source
supplier environment” that exists in the cardiac PET market today and that these initiatives are intended to drive the Company
towards consistent profitability and cash flow.
Results of Operations
Comparison of the Results of Operations
for the Three Months ended March 31, 2014 and 2013
The Company experienced $554,000
net loss for the three months ended March 31, 2015 compared to a net loss of $861,000 for the three months ended March 31, 2014. The
decrease in the loss current three month period as compared to the same period last year is attributed primarily to a decrease
in expenses.
Revenues -
Service and parts Revenues for the three months ended March 31, 2015 were $346,000 as compared to $456,000 for the three
months ended March 31, 2014. Sales of PET systems during the three months ended March 31, 2015 and 2014 have been
negatively impacted by shortage of Sr-82/Rb-82 generators supplied to cardiac imaging facilities by Bracco Diagnostics due
to cyclotron maintenance and limited production capacity of the isotope Sr-82.
Gross Margin -
Gross margin for the three months ended March 31, 2015 and 2014 was $136,000 and $28,000, respectively. The increase is attributable
to a decrease in the number of personnel during the three months ended March 31, 2015.
Operating Expenses
- Operating expenses for the three months ended March 31, 2015 were $667,000 compared to $713,000 for the three months ended
March 31, 2014. The Company reduced personnel through the consolidation of positions.
The Company recorded $120,000
in research and development costs during the three months ended March 31, 2015, compared to $102,000 for the three months ended
March 31, 2014. Research and development costs included mostly payroll, contract labor and consulting fees for the radiopharmaceutical
facility to prepare it for regulatory approvals, production as well as automated devices. The Company intends to continue
to support research and development in radiopharmaceutical products and automated devices.
Sales and marketing expense for the
three months ended March 31, 2015 and 2014 were $42,000 and $46,000, respectively and were lower in 2015 due to the Company’s
efforts to limit expenditures. Sales and marketing expenses for the three months ended March 31, 2015 and 2014 are mostly comprised
of salaries and consulting fees.
General and administrative expenses
during the three months ended March 31, 2015 were $505,000 as compared to $565,000 for the three months ended March 31, 2014. During
the three months ended March 31, 2015 and 2014 the Company recorded $159,000 and $88,000 in stock option expense, respectively.
The Company reduced personnel through consolidation of job positions.
Other Income (Expenses)
- Interest expense was $136,000 for the three months ended March 31, 2015 and includes the $115,000 for the accretion of the
convertible debentures discount and $21,000 for interest payable on the debt. Interest expense was $396,000 for the three months
ended March 31, 2014 and includes the $381,000 for the accretion of the convertible debentures discount and $15,000 for interest
payable on the debt.
During the three months ended
March 31, 2015 and 2014, the Company also recorded derivative gain of $98,000 and $220,000, respectively, in connection with the
embedded conversion derivative liabilities related to convertible debt.
Liquidity and Capital Resources
At March 31, 2015, the Company
had current assets of $596,000 and current liabilities of $2,630,000 compared to December 31, 2014 when the Company had current
assets of $730,000 and current liabilities of $2,697,000. Total assets at March 31, 2015 were $1,685,000 compared to $1,869,000
at December 31, 2014. Total liabilities were $2,638,000 and $2,706,000 at March 31, 2015 and December 31, 2014, respectively.
Cash and cash equivalents at
March 31, 2015 were $79,000 compared to $208,000 at December 31, 2014. Accounts receivable was $164,000 at March 31, 2054 compared
to $175,000 at December 31, 2014.
Current liabilities include
accounts payable and accrued expenses of $807,000 at March 31, 2015.
Net cash used in operating activities
was $336,000 and $695,000 for the three months ended March 31, 2015 and 2014, respectively.
Net cash used in investing activities
were $0 and $2,000 for the three months ended March 31, 2015 and 2014, respectively.
Net cash provided by financing
activities was $207,000 and $131,000 for the three months ended March 31, 2015 and 2014, respectively.
The Company's ability to achieve
its objectives is dependent on its ability to sustain and enhance its revenue stream and to continue to raise funds through loans,
credit and the private placement of restricted securities until such time as the Company achieves profitability. To date, management
has been successful in raising cash on an as-needed basis for the continued operations of the Company. There is no guarantee that
management will be able to continue to raise needed cash in this fashion.
The report of the Company’s
independent public accountants, which accompanied the financial statements for the year ended December 31, 2014, was qualified
with respect to the ability of the Company to continue as a going concern. If the Company is unable to obtain debt or equity financing
to meet its ongoing cash needs, it may have to limit or disregard portions of its business plan.
The Company has no material
commitments for capital expenditures at this time.
Off-Balance Sheet Arrangements
The Company has no “off
balance sheet” source of liquidity arrangements.
ITEM 3 – QUANTITATIVE AND QUALITATIVE
DISCLOSURES ABOUT MARKET RISK
We are a smaller reporting company
as defined by 17 C.F.R. 229 (10)(f)(i) and are not required to provide information under this item.
ITEM 4 – CONTROLS AND PROCEDURES
Evaluation of Disclosure
Controls and Procedures
Based upon an evaluation of
the effectiveness of disclosure controls and procedures, our President and Chief Financial Officer ("CFO") has concluded
that as of the end of the period covered by this Quarterly Report on Form 10-Q our disclosure controls and procedures (as defined
in Rules 13a-15(e) or 15d-15(e) under the Exchange Act) were effective to provide reasonable assurance that information required
to be disclosed in our Exchange Act reports is recorded, processed, summarized and reported within the time periods specified by
the rules and forms of the SEC and is accumulated and communicated to management, including the CFO, as appropriate to allow timely
decisions regarding required disclosure. As reported in our Annual Report on Form 10-K for the year ended December 31, 2014, the
Company’s financial officer has determined that there is a material weakness in our disclosure controls and procedures.
Notwithstanding the foregoing, we have identified
the following material weaknesses in our disclosure procedures:
Audit Committee and Financial
Expert - The Company does not have a formal audit committee with a financial expert, and thus the Company lacks the
board oversight role within the financial reporting process.
Disclosures of Related Party
Transactions – The Company restated its financial statements for each of the first three quarters of 2014
following review of the Company’s related party disclosures during such periods.
The Company intends to enhance its process for classifying
and categorizing transactions by examining all transactions on a monthly basis and communicating such transaction classifications
to the Company’s accountants who prepare the quarterly schedules.
Changes in Internal Control
over Financial Reporting
There have not been any changes
in the Company's internal control over financial reporting (as defined in Rule 13a-15(f)) during the quarter ended March 31, 2015
that have materially affected, or are reasonably likely to materially affect, the Company's internal control over financial reporting.
PART II OTHER INFORMATION
ITEM 1 – LEGAL PROCEEDINGS
On June 8, 2012, the owner of
the radiopharmaceutical manufacturing facility the Company formerly leased in Crown Point, Indiana commenced an action to recover
the use of the premises and the remaining rent due under the lease. On November 14, 2012, the owner was awarded a judgment against
the Company in the amount of $85,525.98 plus interest at the rate of 8%. The Company and the owner agreed to monthly payments in
the minimum amount of $5,000 until the judgment is paid in its entirety. Upon determination of the disposition of the Company’s
security deposit, the terms of the judgment will be completed.
In May, 2013, the Company was
served with a First Amended Complaint in action commenced against its former CEO and principal shareholder. The plaintiff in the
action is seeking to enforce a judgment against the former CEO and principal shareholder and is seeking to have the Company’s
Westmont, Illinois offices, which it purchased from the former CEO, reconveyed. The related party defendants have disputed the
basis of the judgment and the Company has denied the allegations in the Complaint and is defending the action. The Plaintiff recently
filed a motion to amend its complaint to seek the return of $1,917,000 of the funds invested by Solaris, plus interest, from the
Company. The motion has not yet been heard by the court.
On October 8, 2014, the Company
accepted service of a Summons and Complaint in an action commenced by the Securities and Exchange Commission (the “Commission),
in the United States District Court for the Southern District of Florida. The complaint alleges the Company’s former
Chairman, CEO and principal stockholder and the Company engaged in fraudulent activity to manipulate the Company’s stock.
The complaint alleges that the former CEO was involved in compensating a confidential informant, who was a former consultant to
the Company, $1,000 to encourage interest and buying in the Company’s stock. The Commission's complaint alleges that the
defendants violated Section 10(b) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”) and Rules
10b-5(a) and 10b-5(c). The Commission is seeking injunctions from future violations and civil money penalties against the Company.
Without admitting or denying the allegations in the complaint, the Company entered into a settlement with the Commission and agreed
not to violate Section 10(b) and Rule 10b-5(a) and (c) of the Exchange Act and to have the determination of any monetary penalty
be decided in a judicial hearing, which has not yet been scheduled.
From time to time, we are a
party to legal proceedings arising in the ordinary course of business. We are not currently a party to any other legal proceedings
that we believe could have a material adverse effect on financial condition or results of operations.
ITEM 2 – UNREGISTERED
SALES OF EQUITY SECURITIES AND USE OF PROCEEDS
In February 2015, the Company
issued an aggregate of 155,138,888 pre-split shares of Common Stock. 15,000,000 shares were issued for consulting services performed,
an aggregate of 1,250,000 shares were issued upon the conversion of 12,500 shares of the Company’s Series B Convertible Preferred
Stock, and 1,250,000 shares were issued for $250,000.
Unless noted above, the sales
of the securities identified above were made pursuant to privately negotiated transactions that did not involve a public offering
of securities and, accordingly, we believe that these transactions were exempt from the registration requirements of the Securities
Act pursuant to Section 4(2) thereof and rules promulgated there under. Each of the above-referenced investors in our stock represented
to us in connection with their investment that they were “accredited investors” (as defined by Rule 501 under the Securities
Act) and were acquiring the shares for investment and not distribution, that they could bear the risks of the investment and could
hold the securities for an indefinite period of time. The investors received written disclosures that the securities had not been
registered under the Securities Act and that any resale must be made pursuant to a registration or an available exemption from
such registration. All of the foregoing securities are deemed restricted securities for purposes of the Securities Act.
ITEM 3 – DEFAULTS UPON
SENIOR SECURITIES
None
ITEM 4 – MINE SAFETY DISCLOSURES
Not Applicable
ITEM 5 – OTHER INFORMATION
In February 2015, the Company
issued an aggregate of 155,138,888 pre-split shares of Common Stock. 15,000,000 shares were issued for consulting services performed,
an aggregate of 1,250,000 shares were issued upon the conversion of 12,500 shares of the Company’s Series B Convertible Preferred
Stock, and 1,250,000 shares were issued for $250,000.
Unless noted above, the sales of the securities identified above were made pursuant to privately negotiated
transactions that did not involve a public offering of securities and, accordingly, we believe that these transactions were exempt
from the registration requirements of the Securities Act pursuant to Section 4(2) thereof and rules promulgated there under. Each
of the above-referenced investors in our stock represented to us in connection with their investment that they were “accredited
investors” (as defined by Rule 501 under the Securities Act) and were acquiring the shares for investment and not distribution,
that they could bear the risks of the investment and could hold the securities for an indefinite period of time. The investors
received written disclosures that the securities had not been registered under the Securities Act and that any resale must be made
pursuant to a registration or an available exemption from such registration. All of the foregoing securities are deemed restricted
securities for purposes of the Securities Act.
ITEM 6 – EXHIBITS
Exhibit |
|
Description of the Exhibit |
|
|
|
31.1 |
|
Certification of Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.* |
|
|
|
31.2 |
|
Certification of Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.* |
|
|
|
32.1 |
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Certification of Principal Executive Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.** |
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32.2 |
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Certification of Principal Financial Officer pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes Oxley Act of 2002.** |
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101.INS |
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XBRL Instance Document* |
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101.SCH |
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XBRL Taxonomy Extension Schema Document* |
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101.CAL |
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XBRL Taxonomy Extension Calculation Linkbase Document* |
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101.DEF |
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XBRL Taxonomy Extension Definition Linkbase Document* |
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101.LAB |
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XBRL Taxonomy Extension Label Linkbase Document* |
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101.PRE |
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XBRL Taxonomy Extension Presentation Linkbase Document* |
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, the Registrant caused this report to be signed on its behalf by the undersigned, thereunto
duly authorized.
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POSITRON CORPORATION |
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Date: May 15, 2015 |
/s/ Joseph G. Oliverio |
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Joseph G. Oliverio |
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President, Chairman of the Board |
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(principal executive officer) |
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Date: May 15, 2015 |
/s/ Corey Conn |
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Corey Conn |
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Chief Financial Officer |
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(principal accounting officer) |
Exhibit 31.1
Certification Pursuant to
Section 302 of
the Sarbanes-Oxley Act of 2002
I, Joseph G. Oliverio, certify that:
1. |
I have reviewed this quarterly report on Form 10-Q of Positron Corporation (the “Registrant”); |
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the Registrant as of, and for, the periods presented in this report; |
4. |
The Registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the Registrant and have: |
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a) |
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the Registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
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b) |
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
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c) |
Evaluated the effectiveness of the Registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
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d) |
Disclosed in this report any change in the Registrant’s internal control over financial reporting that occurred during the Registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of annual report) that has materially affected, or is reasonably likely to materially affect, the Registrant’s internal control over financial reporting; and |
5. |
The Registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the Registrant’s auditors and the audit committee of the Registrant’s board of directors (or persons performing the equivalent functions): |
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a) |
All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the Registrant’s ability to record, process, summarize and report financial information; and |
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b) |
Any fraud, whether or not material, that involves management or other employees who have a significant role in the Registrant’s internal control over financial reporting. |
Dated: May 15, 2015 |
/s/ Joseph G. Oliverio |
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Joseph G. Oliverio |
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President, Chairman of the Board |
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(principal executive officer) |
Exhibit 31.2
Certification Pursuant to
Section 302 of
the Sarbanes-Oxley Act of 2002
I, Corey Conn, certify that:
1. |
I have reviewed this quarterly report on Form 10-Q of Positron Corporation; |
2. |
Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
3. |
Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the Registrant as of, and for, the periods presented in this report; |
4. |
The Registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the Registrant and have: |
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a) |
Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the Registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
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b) |
Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
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c) |
Evaluated the effectiveness of the Registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
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d) |
Disclosed in this report any change in the Registrant’s internal control over financial reporting that occurred during the Registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of annual report) that has materially affected, or is reasonably likely to materially affect, the Registrant’s internal control over financial reporting; and |
5. |
The Registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the Registrant’s auditors and the audit committee of the Registrant’s board of directors (or persons performing the equivalent functions): |
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a) |
All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the Registrant’s ability to record, process, summarize and report financial information; and |
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b) |
Any fraud, whether or not material, that involves management or other employees who have a significant role in the Registrant’s internal control over financial reporting. |
Dated: May 15, 2015 |
/s/ Corey Conn |
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Corey Conn |
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Chief Financial Officer |
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(principal accounting officer) |
Exhibit 32.1
Certification Pursuant to 18 U.S.C. Section
1350,
As Adopted Pursuant to
Section 906 of the Sarbanes-Oxley Act
of 2002
In connection with the Quarterly Report
of Positron Corporation (the “Registrant”) on Form 10-Q for the fiscal quarter ended March 31, 2015 as filed with the
Securities and Exchange Commission on the date hereof (the “Report”), Joe Oliverio, as Chairman of the Board hereby
certifies, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 that:
(1) The Report fully complies with the
requirements of section 13 (a) or 15 (d), as applicable of the Securities Exchange Act of 1934; and
(2) The information contained in the Report
fairly presents, in all material respects, the financial condition and results of operations of the Registrant.
Dated: May 15, 2015 |
/s/ Joseph G. Oliverio |
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Joseph G. Oliverio |
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President, Chairman of the Board |
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(principal executive officer) |
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A signed original of this written statement
required by Section 906 has been provided to Positron Corporation and will be retained by Positron Corporation and furnished to
the Securities and Exchange Commission or its staff upon request.
Exhibit 32.2
Certification Pursuant to 18 U.S.C. Section
1350,
As Adopted Pursuant to
Section 906 of the Sarbanes-Oxley Act
of 2002
In connection with the Quarterly Report
of Positron Corporation (the “Registrant”) on Form 10-Q for the fiscal quarter ended March 31, 2015 as filed with the
Securities and Exchange Commission on the date hereof (the “Report”), Corey Conn, as Chief Financial Officer hereby
certifies, pursuant to 18 U.S.C. Section 1350, as adopted pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 that:
(1) The Report fully complies with the
requirements of section 13 (a) or 15 (d), as applicable of the Securities Exchange Act of 1934; and
(2) The information contained in the Report
fairly presents, in all material respects, the financial condition and results of operations of the Registrant.
Dated: May 15, 2015 |
/s/ Corey Conn |
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Corey Conn |
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Chief Financial Officer |
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(principal accounting officer) |
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A signed original of this written statement
required by Section 906 has been provided to Positron Corporation and will be retained by Positron Corporation and furnished to
the Securities and Exchange Commission or its staff upon request.
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