Jagen D. Lewicki: Final Debarment Order, 15190-15191 [2020-05449]
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15190
Federal Register / Vol. 85, No. 52 / Tuesday, March 17, 2020 / Notices
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of
responses per
respondent
Number of
respondents
21 CFR section/form
Average
burden per
response
Total annual
responses
Total hours
Total
operating and
maintenance
costs
Color Additive Petitions
70.25, 71.1 ...............................................
2
1
2
1,337
2,674
$5,600
Food Additive Petitions
171.1 ........................................................
Form FDA 3503 .......................................
3
6
1
1
3
6
7,093
1
21,279
6
0
0
Total ..................................................
........................
........................
........................
........................
23,959
5,600
khammond on DSKJM1Z7X2PROD with NOTICES
1 There
are no capital costs associated with this collection of information.
Our estimate of burden attributable to
food additive or color additive petitions
is based on our experience with the
information collection, which has not
changed since our last review, and we
therefore retain the currently approved
burden. This estimate reflects the
average number of petitions we have
received annually over a period of 10
years. The attendant burden we estimate
also reflects an industry average,
although burden associated with
individual petitions may vary
depending on the complexity of the
petition, and the amount and type of
data needed for scientific analysis.
Color additive petitions are subject to
fees. The listing fee for a color additive
petition ranges from $1,600 to $3,000,
depending on the intended use of the
color additive and the scope of the
requested amendment. A complete
schedule of fees is set forth in § 70.19.
An average of one Category A and one
Category B color additive petition is
expected per year. The maximum color
additive petition fee for a Category A
petition is $2,600 and the maximum
color additive petition fee for a Category
B petition is $3,000. Because an average
of 2 CAPs are expected per calendar
year, the estimated total annual cost
burden to petitioners for this startup
cost would be less than or equal to
$5,600 ((1 × $2,600) + (1 × $3,000)
listing fees = $5,600). There are no
capital costs associated with CAPs. The
labeling requirements for food and color
additives were designed to specify the
minimum information needed for
labeling in order that food and color
manufacturers may comply with all
applicable provisions of the FD&C Act
and other specific labeling acts
administered by FDA. Label information
does not require any additional
information gathering beyond what is
already required to assure conformance
with all specifications and limitations in
any given food or color additive
VerDate Sep<11>2014
17:32 Mar 16, 2020
Jkt 250001
regulation. Label information does not
have any specific recordkeeping
requirements unique to preparing the
label. Therefore, because labeling
requirements under § 70.25 for a
particular color additive involve
information required as part of the CAP
safety review process, the estimate for
number of respondents is the same for
§§ 70.25 and 71.1, and the burden hours
for labeling are included in the estimate
for § 71.1. Also, because labeling
requirements under parts 172, 173, 179,
and 180 for particular food additives
involve information required as part of
the FAP safety review process under
§ 171.1, the burden hours for labeling
are included in the estimate for § 171.1.
Dated: March 10, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020–05447 Filed 3–16–20; 8:45 am]
BILLING CODE 4164–01–P
(HGH) imported from China for a
purpose other than the treatment of a
disease or other recognized medical
condition, the use of which had been
authorized by the Secretary of Health
and Human Services, and not pursuant
to an order of a physician, in violation
of the FD&C Act. The factual basis
supporting this felony conviction, as
described below, is conduct relating to
the importation into the United States of
a drug or controlled substance. Mr.
Lewicki was given notice of the
proposed debarment and, in accordance
with the FD&C Act and FDA’s
regulations, was given an opportunity to
request a hearing to show why he
should not be debarred. As of October
28, 2019 (30 days after receipt of the
notice), Mr. Lewicki had not responded.
Mr. Lewicki’s failure to respond and
request a hearing constitutes a waiver of
his right to a hearing concerning this
matter.
This order is applicable March
17, 2020.
ADDRESSES: Submit applications for
termination of debarment to the Dockets
Management Staff, Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Jaime Espinosa, Division of
Enforcement, Office of Strategic
Planning and Operational Policy, Office
of Regulatory Affairs, Food and Drug
Administration, 12420 Parklawn Dr.,
Rockville, MD 20857, or at debarments@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
DATES:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2019–N–3131]
Jagen D. Lewicki: 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
Jagen Lewicki for a period of 5 years
from importing or offering for import
any drug into the United States. FDA
bases this order on a finding that Mr.
Lewicki was convicted, as defined in
the FD&C Act, of one felony count
under Federal law for conspiracy to
distribute Human Growth Hormone
SUMMARY:
PO 00000
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Fmt 4703
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I. Background
Section 306(b)(1)(D) of the FD&C Act
(21 U.S.C. 335a(b)(1)(D)) 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
E:\FR\FM\17MRN1.SGM
17MRN1
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 85, No. 52 / Tuesday, March 17, 2020 / Notices
been convicted of a felony for conduct
relating to the importation into the
United States of any drug or controlled
substance.
On December 20, 2018, Mr. Lewicki
was convicted as defined in section
306(l)(1)(B) of the FD&C Act, in the
United States District Court for the
Eastern District of Virginia, when the
court accepted his plea of guilty for the
offense of conspiracy to distribute HGH
imported from China for unapproved
purposes in violation of 18 U.S.C. 371
and 21 U.S.C. 333(e) (section 303(e) of
FD&C Act).
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 Stipulation
of Facts incorporated into the Plea
Agreement, filed on December 20, 2018,
from on or about January 2017 to
February 2018, Mr. Lewicki conspired
with certain other known and unknown
individuals to unlawfully distribute
HGH imported from China. Specifically,
Mr. Lewicki submitted periodic orders,
and gave money, for HGH to coconspirators, for the purchase of HGH
from manufacturers based in China. In
addition, Mr. Lewicki set up various
post office boxes at private carriers in
the Eastern District of Virginia. The
Chinese based manufacturers delivered
vials of HGH from China to Mr. Lewicki
at post office boxes he set up. Mr.
Lewicki received approximately 90
packages from Chinese manufacturers,
each containing 200 vials of HGH. Mr.
Lewicki would then sell these vials to
individual customers throughout the
United States for bodybuilding and
other unapproved purposes. Mr.
Lewicki’s actions were in violation of 18
U.S.C. 371 and 21 U.S.C. 333(e) (section
303(e) of the FD&C Act).
As a result of this conviction FDA
sent Mr. Lewicki, by certified mail on
September 25, 2019, a notice proposing
to debar him for 5 years from importing
or offering for import any drug into the
United States. The proposal was based
on a finding under section 306(b)(3)(C)
of the FD&C Act that Mr. Lewicki’s
felony conviction for conspiracy in
violation of 18 U.S.C. 371 and section
303(e) of the FD&C Act was for conduct
relating to the importation into the
United States of any drug or controlled
substance because on multiple
occasions, he imported HGH from China
and conspired to distribute it within the
United States. 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. Lewicki’s offense and, for the
reasons detailed in the notice,
VerDate Sep<11>2014
17:32 Mar 16, 2020
Jkt 250001
concluded that his offense warranted a
5-year period of debarment under
section 306(c)(2)(A)(iii).
The proposal informed Mr. Lewicki of
the proposed debarment and offered Mr.
Lewicki 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. Lewicki received the
proposal and notice of opportunity for
a hearing on September 28, 2019. Mr.
Lewicki 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)(3)(C) of the FD&C Act, under
authority delegated to the Assistant
Commissioner, finds that Mr. Lewicki
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. FDA
finds that the offense should be
accorded a debarment period of 5 years.
As a result of the foregoing finding,
pursuant to section 306(b)(1)(D) of the
FD&C Act, Mr. Lewicki is debarred for
a period of 5 years from importing or
offering for import any drug into the
United States, effective (see DATES).
Pursuant to section 301(cc) of the FD&C
Act (21 U.S.C. 331(cc)), the importing or
offering for import into the United
States of any drug by, with the
assistance of, or at the direction of, Mr.
Lewicki is a prohibited act.
Any application by Mr. Lewicki for
termination of debarment under section
306(d)(1) of the FD&C Act should be
identified with Docket No. FDA–2019–
N–3131 and sent to the Dockets
Management Staff (see ADDRESSES). All
such submissions are to be filed in four
copies. 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.
Dated: March 11, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020–05449 Filed 3–16–20; 8:45 am]
BILLING CODE 4164–01–P
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Fmt 4703
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15191
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2019–N–3474]
Zhang Xiao Dong: 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
Zhang Xiao Dong for a period of 5 years
from importing articles of food
(including dietary supplements) or
offering such articles for importation
into the United States. FDA bases this
order on a finding that Mr. Dong was
convicted, as defined in the FD&C Act,
of a felony count under Federal law for
conduct relating to the importation into
the United States of an article of food.
Mr. Dong was given notice of the
proposed permanent debarment and an
opportunity to request a hearing within
the timeframe prescribed by regulation.
As of November 19, 2019 (30 days after
receipt of the notice), Mr. Dong has not
responded. Mr. Dong’s failure to
respond and request a hearing
constitutes a waiver of his right to a
hearing concerning this matter.
DATES: This order is applicable March
17, 2020.
ADDRESSES: Submit applications for
termination of debarment to the Dockets
Management Staff, Food and Drug
Administration, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Jaime Espinosa, Division of
Enforcement, Office of Strategic
Planning and Operational Policy, Office
of Regulatory Affairs, Food and Drug
Administration, 12420 Parklawn Dr.,
Rockville, MD 20857, or at debarments@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
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.
On December 20, 2018, Mr. Dong was
convicted as defined in section
E:\FR\FM\17MRN1.SGM
17MRN1
Agencies
[Federal Register Volume 85, Number 52 (Tuesday, March 17, 2020)]
[Notices]
[Pages 15190-15191]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-05449]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2019-N-3131]
Jagen D. Lewicki: 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
Jagen Lewicki for a period of 5 years from importing or offering for
import any drug into the United States. FDA bases this order on a
finding that Mr. Lewicki was convicted, as defined in the FD&C Act, of
one felony count under Federal law for conspiracy to distribute Human
Growth Hormone (HGH) imported from China for a purpose other than the
treatment of a disease or other recognized medical condition, the use
of which had been authorized by the Secretary of Health and Human
Services, and not pursuant to an order of a physician, in violation of
the FD&C Act. The factual basis supporting this felony conviction, as
described below, is conduct relating to the importation into the United
States of a drug or controlled substance. Mr. Lewicki was given notice
of the proposed debarment and, in accordance with the FD&C Act and
FDA's regulations, was given an opportunity to request a hearing to
show why he should not be debarred. As of October 28, 2019 (30 days
after receipt of the notice), Mr. Lewicki had not responded. Mr.
Lewicki's failure to respond and request a hearing constitutes a waiver
of his right to a hearing concerning this matter.
DATES: This order is applicable March 17, 2020.
ADDRESSES: Submit applications for termination of debarment to the
Dockets Management Staff, Food and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Jaime Espinosa, Division of
Enforcement, Office of Strategic Planning and Operational Policy,
Office of Regulatory Affairs, Food and Drug Administration, 12420
Parklawn Dr., Rockville, MD 20857, or at [email protected].
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(b)(1)(D) of the FD&C Act (21 U.S.C. 335a(b)(1)(D))
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
[[Page 15191]]
been convicted of a felony for conduct relating to the importation into
the United States of any drug or controlled substance.
On December 20, 2018, Mr. Lewicki was convicted as defined in
section 306(l)(1)(B) of the FD&C Act, in the United States District
Court for the Eastern District of Virginia, when the court accepted his
plea of guilty for the offense of conspiracy to distribute HGH imported
from China for unapproved purposes in violation of 18 U.S.C. 371 and 21
U.S.C. 333(e) (section 303(e) of FD&C Act).
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 Stipulation of Facts
incorporated into the Plea Agreement, filed on December 20, 2018, from
on or about January 2017 to February 2018, Mr. Lewicki conspired with
certain other known and unknown individuals to unlawfully distribute
HGH imported from China. Specifically, Mr. Lewicki submitted periodic
orders, and gave money, for HGH to co-conspirators, for the purchase of
HGH from manufacturers based in China. In addition, Mr. Lewicki set up
various post office boxes at private carriers in the Eastern District
of Virginia. The Chinese based manufacturers delivered vials of HGH
from China to Mr. Lewicki at post office boxes he set up. Mr. Lewicki
received approximately 90 packages from Chinese manufacturers, each
containing 200 vials of HGH. Mr. Lewicki would then sell these vials to
individual customers throughout the United States for bodybuilding and
other unapproved purposes. Mr. Lewicki's actions were in violation of
18 U.S.C. 371 and 21 U.S.C. 333(e) (section 303(e) of the FD&C Act).
As a result of this conviction FDA sent Mr. Lewicki, by certified
mail on September 25, 2019, a notice proposing to debar him for 5 years
from importing or offering for import any drug into the United States.
The proposal was based on a finding under section 306(b)(3)(C) of the
FD&C Act that Mr. Lewicki's felony conviction for conspiracy in
violation of 18 U.S.C. 371 and section 303(e) of the FD&C Act was for
conduct relating to the importation into the United States of any drug
or controlled substance because on multiple occasions, he imported HGH
from China and conspired to distribute it within the United States. 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. Lewicki's offense and, for the reasons detailed in the notice,
concluded that his offense warranted a 5-year period of debarment under
section 306(c)(2)(A)(iii).
The proposal informed Mr. Lewicki of the proposed debarment and
offered Mr. Lewicki 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. Lewicki received the proposal and notice of
opportunity for a hearing on September 28, 2019. Mr. Lewicki 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)(3)(C) of the FD&C Act, under
authority delegated to the Assistant Commissioner, finds that Mr.
Lewicki 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. FDA finds that the offense should be accorded a
debarment period of 5 years.
As a result of the foregoing finding, pursuant to section
306(b)(1)(D) of the FD&C Act, Mr. Lewicki is debarred for a period of 5
years from importing or offering for import any drug into the United
States, effective (see DATES). Pursuant to section 301(cc) of the FD&C
Act (21 U.S.C. 331(cc)), the importing or offering for import into the
United States of any drug by, with the assistance of, or at the
direction of, Mr. Lewicki is a prohibited act.
Any application by Mr. Lewicki for termination of debarment under
section 306(d)(1) of the FD&C Act should be identified with Docket No.
FDA-2019-N-3131 and sent to the Dockets Management Staff (see
ADDRESSES). All such submissions are to be filed in four copies. 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.
Dated: March 11, 2020.
Lowell J. Schiller,
Principal Associate Commissioner for Policy.
[FR Doc. 2020-05449 Filed 3-16-20; 8:45 am]
BILLING CODE 4164-01-P