Brian Michael Parks: Final Debarment Order, 8264-8265 [2022-03098]

Download as PDF 8264 Federal Register / Vol. 87, No. 30 / Monday, February 14, 2022 / Notices jspears on DSK121TN23PROD with NOTICES1 report, please visit https://www.fda.gov/ media/154873/download. III. Participating in the Public Meeting Registration: To register for the public meeting, please visit the following website: https://pdufa-hrassessment.eventbrite.com. Please provide complete contact information for each attendee, including name, title, affiliation, address, email, and telephone. Registration is free and based on space availability, with priority given to early registrants. Persons interested in attending this public meeting must register by March 14, 2022, 11:59 p.m. Eastern Time. We will let registrants know if registration closes before the day of the public meeting. If you need special accommodations due to a disability, please contact Patricia Stewart (see FOR FURTHER INFORMATION CONTACT) no later than March 8, 2022. 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Streaming Webcast of the public meeting: The webcast for this public meeting is accessible at https://pdufahr-assessment.eventbrite.com. If you have never attended a Connect Pro event before, test your connection at https://collaboration.fda.gov/common/ help/en/support/meeting_test.htm. To get a quick overview of the Connect Pro program, visit https://www.adobe.com/ go/connectpro_overview. FDA has verified the website addresses in this document, as of the date this document publishes in the Federal Register, but websites are subject to change over time. Transcripts: Please be advised that as soon as a transcript of the public meeting is available, it will be accessible VerDate Sep<11>2014 17:54 Feb 11, 2022 Jkt 256001 at https://www.regulations.gov. It may be viewed at the Dockets Management Staff (see ADDRESSES). Dated: February 9, 2022. Lauren K. Roth, Associate Commissioner for Policy. [FR Doc. 2022–03097 Filed 2–11–22; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2021–N–0304] Brian Michael Parks: Final Debarment Order AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is issuing an order under the Federal Food, Drug, and Cosmetic Act (FD&C Act) debarring Brian Michael Parks for a period of 5 years from importing or offering for import any article of food (including dietary supplements) or drug into the United States. FDA bases this order on a finding that Mr. Parks was convicted of one felony count under Federal law for distribution of an unapproved new drug with the intent to defraud and mislead. The factual basis supporting Mr. Parks’ conviction, as described below, is conduct relating to the importation into the United States of any food and of any drug or controlled substance. Mr. Parks was given notice of the proposed debarment and was given an opportunity to request a hearing to show why he should not be debarred. As of November 17, 2021 (30 days after receipt of the notice), Mr. Parks had not responded. Mr. Parks’ failure to respond and request a hearing constitutes a waiver of his right to a hearing concerning this matter. DATES: This order is applicable February 14, 2022. ADDRESSES: Submit applications for termination of debarment to the Dockets Management Staff, Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240–402– 7500, or at https://www.regulations.gov. FOR FURTHER INFORMATION CONTACT: Jaime Espinosa, Division of Enforcement (ELEM–4029), Office of Strategic Planning and Operational Policy, Office of Regulatory Affairs, Food and Drug Administration, 12420 Parklawn Dr., Rockville, MD 20857, 240–402–8743, or at debarments@fda.hhs.gov. SUPPLEMENTARY INFORMATION: SUMMARY: PO 00000 Frm 00038 Fmt 4703 Sfmt 4703 I. Background Section 306(b)(1)(C) of the FD&C Act (21 U.S.C. 335a(b)(1)(C)) permits FDA to debar an individual from importing an article of food or offering such an article for import into the United States if FDA finds, as required by section 306(b)(3)(A) of the FD&C Act, that the individual has been convicted of a felony for conduct relating to the importation into the United States of any food. Section 306(b)(1)(D) of the FD&C Act permits debarment of an individual from importing or offering for import any drug into the United States if the FDA finds, as required by section 306(b)(3)(C) of the FD&C Act that the individual has been convicted of a felony for conduct relating to the importation into the United States of any drug or controlled substance. On February 16, 2021, Mr. Parks was convicted, as defined in section 306(l)(1) of the FD&C Act in the U.S. District Court for the Western District of Virginia, after his plea of guilty, when the court entered judgment against him for the offense of distribution of an unapproved new drug with the intent to defraud and mislead, in violation of sections 301(d) and 303(a)(2) of the FD&C Act 21 U.S.C. 331(d) and 333(a)(2). The FDA’s finding that debarment is appropriate is based on the felony conviction referenced herein. The factual basis for this conviction is as follows: As contained in the information in Mr. Parks’ case, filed on November 23, 2020, he was the owner and operator of MedFitRX Inc., later known as MedFit Sarmacuticals Inc. (collectively referred to as MedFitRX herein), a purported sport supplement company based in North Carolina. MedFitRX imported Selective Androgen Receptor Modulators (SARMs) in order to use them in MedFitRx products. SARMs are synthetic chemicals designed to mimic the effects of testosterone and other anabolic steroids. From approximately March 2016 to September 2019, Mr. Parks imported SARMs and other drug active ingredients from China on multiple occasions. The drug active ingredients he imported included MK– 677, S–4, MK–2866, GW–501516, LGD– 4033, and RAD140, among others. In addition, on or about May 17, 2018, Mr. Parks sold two MedFitRX products to undercover FDA Office of Criminal Investigation agents posing as consumers. The first product Mr. Parks sold to these undercover agents, Lucky SARMS Magical AF, contained the drugs S–23 and SR9009, which he had caused to be imported into the United States. The second product, Estrovert, E:\FR\FM\14FEN1.SGM 14FEN1 jspears on DSK121TN23PROD with NOTICES1 Federal Register / Vol. 87, No. 30 / Monday, February 14, 2022 / Notices contained the anabolic steroid Methyldienolone, a controlled substance prohibited under the Designer Steroid Act, 21 U.S.C. 802(41), which Mr. Parks also caused to be imported into the United States. Mr. Parks worked with others to conceal the importation of these and other unapproved drugs as they were disguised and misdeclared as articles of food, specifically ‘‘biscuit mix powder,’’ ‘‘corn powder,’’ ‘‘grain mix powder,’’ ‘‘bread mix powder,’’ and ‘‘milk tea powder.’’ Mr. Parks then included these drug active ingredients in MedFitRX products, which were unapproved drugs that he introduced and delivered for introduction into interstate commerce. Mr. Parks knowingly marketed these MedFitRX products as ‘‘dietary supplements’’ and ‘‘sports supplements’’ to create the impression they were safe and legal to use, and otherwise intentionally failed to include certain drug active ingredients on the product labels. As a result of this conviction, FDA sent Mr. Parks, by certified mail, on October 12, 2021, a notice proposing to debar him for a 5-year period from importing or offering for import any article of food or drug into the United States. The proposal was based on a finding under section 306(b)(1)(C) and (b)(3)(C) of the FD&C Act that Mr. Parks’ felony conviction of distribution of an unapproved new drug with the intent to defraud and mislead constitutes conduct relating to the importation into the United States of an article of food and any drug or controlled substance because Mr. Parks illegally imported unapproved drugs into the United States, working with others to disguise and misdeclare them as articles of food, and then distributed those unapproved drugs to consumers in the United States, marketing them as ‘‘dietary supplements’’ and ‘‘sports supplements.’’ In proposing a debarment period, FDA weighed the considerations set forth in section 306(c)(3) of the FD&C Act that it considered applicable to Mr. Parks’ offense, and concluded that the felony offense warranted the imposition of a 5year period of debarment. The proposal informed Mr. Parks of the proposed debarment and offered him an opportunity to request a hearing, providing him 30 days from the date of receipt of the letter in which to file the request, and advised him that failure to request a hearing constituted a waiver of the opportunity for a hearing and of any contentions concerning this action. Mr. Parks received the proposal and notice of opportunity for a hearing on October 18, 2021. Mr. Parks failed to request a hearing within the timeframe prescribed VerDate Sep<11>2014 17:54 Feb 11, 2022 Jkt 256001 by regulation and has, therefore, waived his opportunity for a hearing and waived any contentions concerning his debarment (21 CFR part 12). II. Findings and Order Therefore, the Assistant Commissioner, Office of Human and Animal Food Operations, under section 306(b)(1)(C) and (b)(3)(C) of the FD&C Act, under authority delegated to the Assistant Commissioner, finds that Mr. Brian Michael Parks has been convicted of a felony under Federal law for conduct relating to the importation into the United States of an article of food and of a drug or controlled substance, and that he is subject to a 5-year period of debarment. As a result of the foregoing finding, Mr. Parks is debarred for a period of 5 years from importing or offering for import articles of food or any drug or controlled substances into the United States, applicable (see DATES). Pursuant to section 301(cc) of the FD&C Act, the importing or offering for import into the United States of an article of food or of any drug or controlled substance by, with the assistance of, or at the direction of Mr. Parks is a prohibited act. Any application by Mr. Parks for termination of debarment under section 306(d)(1) of the FD&C Act should be identified with Docket No. FDA–2021– N–0304 and sent to the Dockets Management Staff (see ADDRESSES). The public availability of information in these submissions is governed by 21 CFR 10.20. Publicly available submissions will be placed in the docket and will be viewable at https://www.regulations.gov or at the Dockets Management Staff (see ADDRESSES) between 9 a.m. and 4 p.m., Monday through Friday, 240–402–7500. Dated: February 8, 2022. Lauren K. Roth, Associate Commissioner for Policy. [FR Doc. 2022–03098 Filed 2–11–22; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Meeting of the Advisory Committee on Infant and Maternal Mortality (Formerly the Advisory Committee on Infant Mortality) Health Resources and Services Administration (HRSA), Department of Health and Human Services. ACTION: Notice. AGENCY: PO 00000 Frm 00039 Fmt 4703 Sfmt 4703 8265 In accordance with the Federal Advisory Committee Act, this notice announces that the Advisory Committee on Infant and Maternal Mortality (ACIMM or Committee) has scheduled a public meeting. Information about ACIMM and the agenda for this meeting can be found on the ACIMM website at https://www.hrsa.gov/ advisory-committees/infant-mortality/ index.html. SUMMARY: March 15, 2022, 12:00 p.m. to 4:00 p.m. Eastern Time and March 16, 2022, 12:00 p.m. to 4:00 p.m. Eastern Time. DATES: This meeting will be held virtually via webinar. The webinar link and log-in information will be available at the ACIMM website before the meeting: https://www.hrsa.gov/advisorycommittees/infant-mortality/. FOR FURTHER INFORMATION CONTACT: Anne Leitch, Maternal and Child Health Bureau, HRSA, 5600 Fishers Lane, Rockville, Maryland 20857; 301–443– 1321; or SACIM@hrsa.gov. SUPPLEMENTARY INFORMATION: ACIMM is authorized by section 222 of the Public Health Service Act (42 U.S.C. 217a), as amended. The Committee is governed by provisions of Public Law 92–463, as amended, (5 U.S.C. App. 2), which sets forth standards for the formation and use of Advisory Committees. The ACIMM advises the Secretary of Health and Human Services (Secretary) on department activities, partnerships, policies, and programs directed at reducing infant mortality, maternal mortality and severe maternal morbidity, and improving the health status of infants and women before, during, and after pregnancy. The Committee provides advice on how to coordinate federal, state, local, tribal, and territorial governmental efforts designed to improve infant mortality, related adverse birth outcomes, and maternal health, as well as influence similar efforts in the private and voluntary sectors. The Committee provides guidance and recommendations on the policies, programs, and resources required to address the disparities and inequities in infant mortality, related adverse birth outcomes and maternal health outcomes, including maternal mortality and severe maternal morbidity. With its focus on underlying causes of the disparities and inequities seen in birth outcomes for women and infants, the Committee advises the Secretary on the health, social, economic, and environmental factors contributing to the inequities and proposes structural, policy, and/or systems level changes. ADDRESSES: E:\FR\FM\14FEN1.SGM 14FEN1

Agencies

[Federal Register Volume 87, Number 30 (Monday, February 14, 2022)]
[Notices]
[Pages 8264-8265]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-03098]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2021-N-0304]


Brian Michael Parks: Final Debarment Order

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is issuing an order 
under the Federal Food, Drug, and Cosmetic Act (FD&C Act) debarring 
Brian Michael Parks for a period of 5 years from importing or offering 
for import any article of food (including dietary supplements) or drug 
into the United States. FDA bases this order on a finding that Mr. 
Parks was convicted of one felony count under Federal law for 
distribution of an unapproved new drug with the intent to defraud and 
mislead. The factual basis supporting Mr. Parks' conviction, as 
described below, is conduct relating to the importation into the United 
States of any food and of any drug or controlled substance. Mr. Parks 
was given notice of the proposed debarment and was given an opportunity 
to request a hearing to show why he should not be debarred. As of 
November 17, 2021 (30 days after receipt of the notice), Mr. Parks had 
not responded. Mr. Parks' failure to respond and request a hearing 
constitutes a waiver of his right to a hearing concerning this matter.

DATES: This order is applicable February 14, 2022.

ADDRESSES: Submit applications for termination of debarment to the 
Dockets Management Staff, Food and Drug Administration, 5630 Fishers 
Lane, Rm. 1061, Rockville, MD 20852, 240-402-7500, or at https://www.regulations.gov.

FOR FURTHER INFORMATION CONTACT: Jaime Espinosa, Division of 
Enforcement (ELEM-4029), Office of Strategic Planning and Operational 
Policy, Office of Regulatory Affairs, Food and Drug Administration, 
12420 Parklawn Dr., Rockville, MD 20857, 240-402-8743, or at 
[email protected].

SUPPLEMENTARY INFORMATION:

I. Background

    Section 306(b)(1)(C) of the FD&C Act (21 U.S.C. 335a(b)(1)(C)) 
permits FDA to debar an individual from importing an article of food or 
offering such an article for import into the United States if FDA 
finds, as required by section 306(b)(3)(A) of the FD&C Act, that the 
individual has been convicted of a felony for conduct relating to the 
importation into the United States of any food. Section 306(b)(1)(D) of 
the FD&C Act permits debarment of an individual from importing or 
offering for import any drug into the United States if the FDA finds, 
as required by section 306(b)(3)(C) of the FD&C Act that the individual 
has been convicted of a felony for conduct relating to the importation 
into the United States of any drug or controlled substance.
    On February 16, 2021, Mr. Parks was convicted, as defined in 
section 306(l)(1) of the FD&C Act in the U.S. District Court for the 
Western District of Virginia, after his plea of guilty, when the court 
entered judgment against him for the offense of distribution of an 
unapproved new drug with the intent to defraud and mislead, in 
violation of sections 301(d) and 303(a)(2) of the FD&C Act 21 U.S.C. 
331(d) and 333(a)(2). The FDA's finding that debarment is appropriate 
is based on the felony conviction referenced herein. The factual basis 
for this conviction is as follows:
    As contained in the information in Mr. Parks' case, filed on 
November 23, 2020, he was the owner and operator of MedFitRX Inc., 
later known as MedFit Sarmacuticals Inc. (collectively referred to as 
MedFitRX herein), a purported sport supplement company based in North 
Carolina. MedFitRX imported Selective Androgen Receptor Modulators 
(SARMs) in order to use them in MedFitRx products. SARMs are synthetic 
chemicals designed to mimic the effects of testosterone and other 
anabolic steroids. From approximately March 2016 to September 2019, Mr. 
Parks imported SARMs and other drug active ingredients from China on 
multiple occasions. The drug active ingredients he imported included 
MK-677, S-4, MK-2866, GW-501516, LGD-4033, and RAD140, among others. In 
addition, on or about May 17, 2018, Mr. Parks sold two MedFitRX 
products to undercover FDA Office of Criminal Investigation agents 
posing as consumers. The first product Mr. Parks sold to these 
undercover agents, Lucky SARMS Magical AF, contained the drugs S-23 and 
SR9009, which he had caused to be imported into the United States. The 
second product, Estrovert,

[[Page 8265]]

contained the anabolic steroid Methyldienolone, a controlled substance 
prohibited under the Designer Steroid Act, 21 U.S.C. 802(41), which Mr. 
Parks also caused to be imported into the United States. Mr. Parks 
worked with others to conceal the importation of these and other 
unapproved drugs as they were disguised and misdeclared as articles of 
food, specifically ``biscuit mix powder,'' ``corn powder,'' ``grain mix 
powder,'' ``bread mix powder,'' and ``milk tea powder.'' Mr. Parks then 
included these drug active ingredients in MedFitRX products, which were 
unapproved drugs that he introduced and delivered for introduction into 
interstate commerce. Mr. Parks knowingly marketed these MedFitRX 
products as ``dietary supplements'' and ``sports supplements'' to 
create the impression they were safe and legal to use, and otherwise 
intentionally failed to include certain drug active ingredients on the 
product labels.
    As a result of this conviction, FDA sent Mr. Parks, by certified 
mail, on October 12, 2021, a notice proposing to debar him for a 5-year 
period from importing or offering for import any article of food or 
drug into the United States. The proposal was based on a finding under 
section 306(b)(1)(C) and (b)(3)(C) of the FD&C Act that Mr. Parks' 
felony conviction of distribution of an unapproved new drug with the 
intent to defraud and mislead constitutes conduct relating to the 
importation into the United States of an article of food and any drug 
or controlled substance because Mr. Parks illegally imported unapproved 
drugs into the United States, working with others to disguise and 
misdeclare them as articles of food, and then distributed those 
unapproved drugs to consumers in the United States, marketing them as 
``dietary supplements'' and ``sports supplements.'' In proposing a 
debarment period, FDA weighed the considerations set forth in section 
306(c)(3) of the FD&C Act that it considered applicable to Mr. Parks' 
offense, and concluded that the felony offense warranted the imposition 
of a 5-year period of debarment.
    The proposal informed Mr. Parks of the proposed debarment and 
offered him an opportunity to request a hearing, providing him 30 days 
from the date of receipt of the letter in which to file the request, 
and advised him that failure to request a hearing constituted a waiver 
of the opportunity for a hearing and of any contentions concerning this 
action. Mr. Parks received the proposal and notice of opportunity for a 
hearing on October 18, 2021. Mr. Parks failed to request a hearing 
within the timeframe prescribed by regulation and has, therefore, 
waived his opportunity for a hearing and waived any contentions 
concerning his debarment (21 CFR part 12).

II. Findings and Order

    Therefore, the Assistant Commissioner, Office of Human and Animal 
Food Operations, under section 306(b)(1)(C) and (b)(3)(C) of the FD&C 
Act, under authority delegated to the Assistant Commissioner, finds 
that Mr. Brian Michael Parks has been convicted of a felony under 
Federal law for conduct relating to the importation into the United 
States of an article of food and of a drug or controlled substance, and 
that he is subject to a 5-year period of debarment.
    As a result of the foregoing finding, Mr. Parks is debarred for a 
period of 5 years from importing or offering for import articles of 
food or any drug or controlled substances into the United States, 
applicable (see DATES). Pursuant to section 301(cc) of the FD&C Act, 
the importing or offering for import into the United States of an 
article of food or of any drug or controlled substance by, with the 
assistance of, or at the direction of Mr. Parks is a prohibited act.
    Any application by Mr. Parks for termination of debarment under 
section 306(d)(1) of the FD&C Act should be identified with Docket No. 
FDA-2021-N-0304 and sent to the Dockets Management Staff (see 
ADDRESSES). The public availability of information in these submissions 
is governed by 21 CFR 10.20.
    Publicly available submissions will be placed in the docket and 
will be viewable at https://www.regulations.gov or at the Dockets 
Management Staff (see ADDRESSES) between 9 a.m. and 4 p.m., Monday 
through Friday, 240-402-7500.

    Dated: February 8, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022-03098 Filed 2-11-22; 8:45 am]
BILLING CODE 4164-01-P


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