[Federal Register Volume 90, Number 5 (Wednesday, January 8, 2025)]
[Notices]
[Pages 1505-1508]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-00126]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2024-N-0604]
Yong Sheng Jiao; Denial of Hearing; Final Debarment Order
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA or Agency) is denying a
request for a hearing submitted by Yong Sheng Jiao, also known as
Yongsheng Jiao and Wilson Jiao (Jiao), and is issuing an order under
the Federal Food, Drug, and Cosmetic Act (FD&C Act) debarring Jiao for
5 years from importing or offering for import any drug into the United
States. FDA bases this order on a finding that Jiao was convicted of a
felony under Federal law for conduct relating to the importation into
the United States of any drug or controlled substance under the FD&C
Act. In determining the appropriateness and period of Jiao's debarment,
FDA considered the relevant factors listed in the FD&C Act. Jiao
submitted a request for hearing but failed to file with the Agency
information and analyses sufficient to create a basis for a hearing.
DATES: The order is applicable January 8, 2025.
ADDRESSES: Any application for termination of debarment by Jiao under
section 306(d) of the FD&C Act (21 U.S.C. 335a(d)) (application) may be
submitted as follows:
Electronic Submissions
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments. An application
submitted electronically, including attachments, to https://www.regulations.gov will be posted to the docket unchanged. Because
your application will be made public, you are solely responsible for
ensuring that your application does not include any confidential
information that you or a third party may not wish to be posted, such
as medical information, your or
[[Page 1506]]
anyone else's Social Security number, or confidential business
information, such as a manufacturing process. Please note that if you
include your name, contact information, or other information that
identifies you in the body of your application, that information will
be posted on https://www.regulations.gov.
If you want to submit an application with confidential
information that you do not wish to be made available to the public,
submit the application as a written/paper submission and in the manner
detailed (see ``Written/Paper Submissions'' and ``Instructions'').
Written/Paper Submissions
Submit written/paper submissions as follows:
Mail/Hand delivery/Courier (for written/paper
submissions): Dockets Management Staff (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852.
For a written/paper application submitted to the Dockets
Management Staff, FDA will post your application, as well as any
attachments, except for information submitted, marked, and identified,
as confidential, if submitted as detailed in ``Instructions.''
Instructions: All applications must include the Docket No. FDA-
2024-N-0604. An application will be placed in the docket and, unless
submitted as ``Confidential Submissions,'' publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m.
and 4 p.m., Monday through Friday, 240-402-7500.
Confidential Submissions--To submit an application with
confidential information that you do not wish to be made publicly
available, submit your application only as a written/paper submission.
You should submit two copies total. One copy will include the
information you claim to be confidential with a heading or cover note
that states ``THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.'' The
Agency will review this copy, including the claimed confidential
information, in its consideration of your application. The second copy,
which will have the claimed confidential information redacted/blacked
out, will be available for public viewing and posted on https://www.regulations.gov. Submit both copies to the Dockets Management
Staff. If you do not wish your name and contact information to be made
publicly available, you can provide this information on the cover sheet
and not in the body of your application and you must identify this
information as ``confidential.'' Any information marked as
``confidential'' will not be disclosed except in accordance with 21 CFR
10.20 and other applicable disclosure law. For more information about
FDA's posting of comments to public dockets, see 80 FR 56469, September
18, 2015, or access the information at: https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf.
Docket: For access to the docket, go to https://www.regulations.gov
and insert the docket number, found in brackets in the heading of this
document, into the ``Search'' box and follow the prompts and/or go to
the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville,
MD 20852 between 9 a.m. and 4 p.m., Monday through Friday, 240-402-
7500. Publicly available submissions may be seen in the docket.
FOR FURTHER INFORMATION CONTACT: Karen Fikes, Office of Scientific
Integrity, Food and Drug Administration, 10903 New Hampshire Ave.,
Bldg. 1, Rm. 4232, Silver Spring, MD 20993, 301-796-9603.
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(b)(1) of the FD&C Act permits FDA to debar an
individual if the Agency finds that the individual has been convicted
of a felony under Federal law for conduct relating to the importation
into the United States of any drug or controlled substance. On January
24, 2023, Jiao, the owner and operator of Santec Chemicals Corporation
and Syntec Pharma Corporation, pled guilty to a felony count of causing
the delivery of misbranded drugs into interstate commerce in violation
of sections 301(a), 303(a)(2), and 502(a) of the FD&C Act (21 U.S.C.
331(a), 333(a)(2), and 352(a)). Then, on January 8, 2024, the U.S.
District Court for the Eastern District of New York entered a judgment
convicting and sentencing Jiao to 2 years of probation and fines.
Jiao's conviction stemmed from conduct, occurring on or about and
between November 30, 2017, and April 30, 2020, relating to the
importation of a drug, dipyrone, which is not approved for use in the
United States. Jiao imported dipyrone from suppliers located in China
into the United States, addressed to one of his businesses, Santec
Chemicals Corporation. The shipments of dipyrone were misbranded in
that they were either not labeled or they were falsely labeled as
sebacic acid. Jiao pled guilty to knowingly and intentionally
introducing into interstate commerce, with the intent to defraud and
mislead the Federal Government, the misbranded drug dipyrone.
By letter dated March 18, 2024, FDA's Office of Regulatory Affairs
(ORA) notified Jiao of its proposal to debar him for a period of 5
years (Proposal). As explained in the Proposal, Jiao's conviction
stemmed from conduct relating to the importation of any drug or
controlled substance into the Unites States by illegally importing and
introducing misbranded dipyrone into interstate commerce in violation
of sections 301(a), 303(a)(2), and 502(a) of the FD&C Act. An
individual convicted of a felony for conduct related to the importation
into the United States of any drug or controlled substance may be
subject to debarment as set forth in section 306(b)(3)(C) of the FD&C
Act. Therefore, ORA found, on the basis of Jiao's conviction, that Jiao
is subject to debarment under section 306(b)(1) of the FD&C Act.
The Proposal explained that the maximum period of debarment for an
individual subject to permissive debarment for a felony under section
306(c)(2)(A)(iii) of the FD&C Act is 5 years. The Proposal also
outlined findings concerning the three relevant factors that ORA
considered in determining the appropriateness and period of debarment,
as provided in section 306(c)(3) of the FD&C Act: (1) the nature and
seriousness of any offense involved; (2) the nature and extent of
voluntary steps to mitigate the impact on the public of any offense
involved; and (3) prior convictions under the FD&C Act or under other
Acts involving matters within the jurisdiction of FDA. ORA found that
the nature and seriousness of the offense and the nature and extent of
voluntary steps to mitigate the effect on the public are unfavorable
factors for Jiao. ORA found the lack of prior convictions involving
matters within FDA jurisdiction as a favorable factor for Jiao. ORA
concluded that the facts supporting the unfavorable factors outweigh
those supporting the favorable factor, thereby warranting a 5-year
period of debarment. The Proposal also informed Jiao of an opportunity
to request a hearing under section 306(i) of the FD&C Act and part 12
(21 CFR part 12).
In response to the Proposal, Jiao submitted a timely request for a
hearing, which included a notice of appearance and a statement of
intent to prepare and submit materials in support of the hearing
request. In a letter submitted to the Dockets Management Staff dated
May 12, 2024, Jiao submitted information in support of his request for
a hearing (Response). Jiao's Response included multiple documents meant
to address the two unfavorable factors identified in ORA's Proposal.
[[Page 1507]]
Under the authority delegated to him by the Commissioner of Food
and Drugs, the Director, Office of Scientific Integrity (OSI Director)
has considered Jiao's request for a hearing. Hearings are granted only
if there is a genuine and substantial issue of fact. A request for a
hearing may not rest upon mere allegations or denials but must present
specific facts showing that there is a genuine and substantial issue of
fact that justifies a hearing. Hearings will not be granted on issues
of policy or law, on mere allegations, denials or general descriptions
of positions and contentions, or on data and information insufficient
to justify the factual determination urged (see 21 CFR 12.24(b)). The
OSI Director has considered Jiao's arguments and concluded that they
are unpersuasive and fail to raise a genuine and substantial issue of
fact requiring a hearing.
II. Argument in Support of a Hearing
Jiao's Response included documents and claims that challenge ORA's
proposed findings in determining the appropriateness and period of
permissive debarment. Specifically, Jiao argues that he should not be
``punished'' for wrongdoing by his company's supplier in China and that
he incorrectly signed the plea agreement due to a misunderstanding,
contending that FDA approved bulk importation of dipyrone during the
time of his illegal importation. As a preliminary matter, debarment,
under section 306 of the FD&C Act, is a remedial measure to protect
public health, not a punishment. (See DiCola v. FDA, 77 F.3d 504, 507
(D.C. Cir. 1996) (permanent debarment of convicted individual is not
punishment, but instead is a remedy to protect the integrity of the
drug industry and public confidence in that industry)). Insofar as Jiao
is arguing that he is actually innocent of the offense to which he pled
guilty, under section 306(l) of the FD&C Act a person is convicted of a
criminal offense, inter alia, when a Federal court enters a judgment of
conviction or when a Federal court accepts a plea of guilty. The
administrative record, including Jiao's supporting documents,
establishes that he pled guilty in Federal court on January 24, 2023.
After accepting Jiao's guilty plea, the Federal court entered a
judgment of conviction on January 8, 2024. Jiao does not dispute the
court's judgment of conviction or acceptance of his guilty plea based
on his admission to knowingly and intentionally importing misbranded
dipyrone with an intent to defraud or mislead the Federal Government.
Jiao cannot now dispute the facts to which he admitted in support of
his guilty plea during the criminal proceedings against him. Federal
court is the proper venue for any challenge to Jiao's guilty plea based
on a claim of actual innocence, not this remedial proceeding.
Jiao next appears to challenge the proposed period of debarment,
arguing that the two considerations in section 306(c)(3) of the FD&C
Act deemed unfavorable in the Proposal should be treated as favorable
in light of the arguments and documents submitted by him in support of
his hearing request.
Relying on the Presentence Investigation Report, Plea Agreement,
and Mitigation Letter from his criminal proceedings, Jiao first appears
to challenge ORA's findings regarding the nature and seriousness of his
offense under section 306(c)(3)(A) of the FD&C Act. Jiao contends that,
as reflected in the documents from his criminal proceedings, his
supplier in China is the cause of shipping the dipyrone as sebacic acid
to avoid the ``unreasonable testing requirement in China'' and that he
relabeled the product before shipment to customers. As noted above,
however, Jiao pled guilty to causing the introduction of a misbranded
drug into the United States. The basis for Jiao's guilty plea was his
causing a misbranded drug to enter the United States, not the
subsequent shipment to his customers. Without FDA premarket review,
such illegally imported drugs pose a significant risk to patients
because they lack findings of safety and effectiveness, manufacturing
quality standards, and appropriate labeling for use. Inasmuch as Jiao
admitted, as part of his guilty plea, to ``knowingly, intentionally,
and voluntarily'' causing the introduction of such drugs into the
United States with an intent to defraud or mislead the Federal
Government, Jiao's claims that his supplier was responsible for
shipping the misbranded product and that he relabeled the product
before further shipment fail to raise a genuine and substantial issue
of fact regarding the nature and seriousness of his offense under
section 306(c)(3)(A) of the FD&C Act, and the OSI Director will treat
this consideration as unfavorable.
Jiao also argues that FDA should treat as favorable the
consideration under section 306(c)(3)(C) of the FD&C Act, which
requires the Agency to consider ``the nature and extent of voluntary
steps to mitigate the impact on the public of any offense involved'' in
determining the appropriateness and period of his debarment. Citing a
Federal Register document from 2019 (84 FR 64080, November 20, 2019),
Jiao argues that FDA ``allowed'' dipyrone for bulk importation and
that, therefore, his company's sales after 2019 should not have created
a negative ``impact on the public.'' Jiao's reading of this Federal
Register document is incorrect. FDA did not indicate in this Federal
Register document that the Agency was either approving, or exercising
enforcement discretion with respect to bulk dipyrone for use in
compounding under limited circumstances. Regardless, as discussed
above, Jiao admitted to knowingly and intentionally importing a
misbranded drug with an intent to defraud or mislead the Federal
Government. Any change in FDA's enforcement policies with respect to
that drug would not qualify as a voluntary step taken by Jiao to
mitigate the impact of his offense on the public, nor does he provide
adequate information regarding additional steps he took that mitigate
the effects of the offenses he committed on the public under section
306(c)(3)(C) of the FD&C Act, and thus, he has a failed to raise a
genuine and substantial issue of fact with respect to that
consideration.
Furthermore, insofar as Jiao intends to argue that FDA's policies
regarding dipyrone at the time of his criminal conduct diminish the
nature and seriousness of his offense, he has also failed to raise a
genuine and substantial issue of fact with respect to the consideration
under section 306(c)(3)(A) of the FD&C Act. As set forth above, he has
mischaracterized FDA's enforcement policies regarding dipyrone at the
time of his criminal conduct. More importantly, as part of his guilty
plea, he admitted to intentionally and knowingly causing the
introduction of a misbranded drug into the United States with an intent
to defraud or mislead the Federal Government. Even assuming that FDA
might have exercised its enforcement discretion with respect to that
drug under a narrow set of circumstances, his own criminal conduct
prevented the Agency from assessing those circumstances with respect to
the drug he offered for import into the United States.
Based on the undisputed record, including the facts to which Jiao
pled guilty in his criminal proceedings, a 5-year debarment period is
appropriate. Although it is undisputed that Jiao has no previous
criminal convictions related to matters within the jurisdiction of FDA,
this single favorable factor does not counterbalance the nature and
seriousness of his offense and lack of voluntary steps promptly taken
to mitigate the impact of his offense on the public. Therefore, the OSI
Director agrees with ORA's conclusion that ``the
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facts supporting the unfavorable factors outweigh those supporting the
favorable factor, and therefore warrant imposition of a five-year
period of debarment.''
III. Findings and Order
Therefore, the OSI Director, under section 306(b)(1) of the FD&C
Act and authority delegated to him by the Commissioner of Food and
Drugs, finds that Jiao has been convicted of a felony under Federal law
for conduct relating to the importation into the United States of any
drug or controlled substance and is subject to debarment, as set forth
in section 306(b)(3)(C) of the FD&C Act. FDA has considered the
applicable factors listed in section 306(c)(3) of the FD&C Act and
determined that a debarment period of 5 years is appropriate.
As a result of the foregoing finding, Jiao is debarred for a period
of 5 years from importing or offering for import any drug into the
United States, effective January 8, 2025. Pursuant to section 301(cc)
of the FD&C Act, the importing or offering for import into the United
States of any drug by, with the assistance of, or at the direction of
Jiao, is a prohibited act.
Dated: December 31, 2024.
George M. Warren,
Director, Office of Scientific Integrity.
[FR Doc. 2025-00126 Filed 1-7-25; 8:45 am]
BILLING CODE 4164-01-P