Kevin Xu: Debarment Order, 17927-17928 [2010-8023]
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17927
Federal Register / Vol. 75, No. 67 / Thursday, April 8, 2010 / Notices
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: ORR Requirements for Refugee
Cash Assistance; and Refugee Medical
Assistance (45 CFR part 400).
OMB No.: 0970–0036.
Description: As required by section
412(e) of the Immigration and
Nationality Act, the Administration for
Children and Families (ACF), Office of
Refugee Resettlement (ORR), is
requesting the information from Form
Dated: April 5, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–7985 Filed 4–7–10; 8:45 am]
BILLING CODE 4184–01–P
ORR–6 to determine the effectiveness of
the State cash and medical assistance,
social services, and targeted assistance
programs. State-by-State Refugee Cash
Assistance (RCA) and Refugee Medical
Assistance (RMA) utilization rates
derived from Form ORR–6 are
calculated for use in formulating
program initiatives, priorities,
standards, budget requests, and
assistance policies. ORR regulations
require that State Refugee Resettlement
and Wilson-Fish agencies, and local and
Tribal governments complete Form
ORR–6 in order to participate in the
above-mentioned programs.
Respondents: State Refugee
Resettlement and Wilson-Fish Agencies,
local, and Tribal governments.
ANNUAL BURDEN ESTIMATES
Number of respondents
Number of responses per
respondent
Average burden hours per
response
Total burden hours
ORR–6
sroberts on DSKD5P82C1PROD with NOTICES
Instrument
50
3
3.88
582
Estimated Total Annual Burden
Hours: 582
In compliance with the requirements
of section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
VerDate Nov<24>2008
16:26 Apr 07, 2010
Jkt 220001
Dated: April 5, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–7983 Filed 4–7–10; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2009–N–0286]
Kevin Xu: 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 (the act) permanently
debarring Kevin Xu from providing
services in any capacity to a person that
has an approved or pending drug
product application. FDA bases this
order on a finding that Mr. Xu was
convicted of a felony under Federal law
for conduct relating to the regulation of
a drug product under the act. Mr. Xu
was given notice of the proposed
permanent debarment and an
opportunity to request a hearing within
the timeframe prescribed by regulation.
As of September 23, 2009, Mr. Xu has
failed to respond. Mr. Xu’s failure to
respond constitutes a waiver of his right
to a hearing concerning this action.
DATES: This order is effective April 8,
2010.
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
ADDRESSES: Submit applications for
special termination of debarment to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852.
FOR FURTHER INFORMATION CONTACT:
Kenny Shade, Division of Compliance
Policy (HFC–230), Office of
Enforcement, Office of Regulatory
Affairs, Food and Drug Administration,
5600 Fishers Lane, Rockville, MD
20857, 240–632–6844.
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(a)(2)(B) of the act (21
U.S.C. 335a(a)(2)(B)) requires debarment
of an individual if FDA finds that the
individual has been convicted of a
felony under Federal law for conduct
otherwise relating to the regulation of
any drug product under the act.
On January 20, 2009, the U.S. District
Court for the Southern District of Texas
entered judgment against Mr. Xu for one
count of participating in a conspiracy to
traffic and attempt to traffic in
counterfeit goods, to cause the
introduction and delivery for
introduction of misbranded prescription
drugs into interstate commerce, and to
cause the counterfeiting of trademarks
in violation of 18 U.S.C. 371, three
counts of causing the introduction and
delivery for introduction of misbranded
prescription drugs into interstate
commerce in violation of 21 U.S.C.
331(a) and 21 U.S.C. 333(a)(2), and one
count of trafficking in counterfeit goods
E:\FR\FM\08APN1.SGM
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sroberts on DSKD5P82C1PROD with NOTICES
17928
Federal Register / Vol. 75, No. 67 / Thursday, April 8, 2010 / Notices
in violation of 18 U.S.C. 2320(a) and 18
U.S.C. 2320(a)(2).
FDA’s finding that debarment is
appropriate is based on the felony
convictions referenced herein for
conduct relating to the regulation of a
drug product. The factual basis for those
convictions is as follows: From July
2006 until on or about July 2007, Mr. Xu
did knowingly, intentionally, and
willfully conspire and agree with other
persons to import pharmaceutical drug
products that bore the trademarks
ZYPREXA, TAMIFLU, CASODEX,
PLAVIX, and ARICEPT without the
authorization of the manufacturer of
these drugs, and then to resell these
products to the public.
On or about December 8, 2007, Mr. Xu
used an Internet email address to send
an email listing the tracking numbers
connected to the sale of counterfeit
pharmaceuticals. On or about April 9,
2007, Mr. Xu caused coconspirators
residing in the Republic of China to
place in interstate commerce for
shipment to the United States various
blister strips containing counterfeit
TAMIFLU, CASODEX, ZYPREXA, and
PLAVIX.
On or about December 8, 2006, with
the intent to defraud or mislead, Mr. Xu
caused the introduction and delivery for
introduction into interstate commerce of
drugs that were misbranded, namely a
shipment containing blister strips of
TAMIFLU capsules that were labeled in
a manner to falsely represent that these
blister strips contained genuine
TAMIFLU.
On or about January 3, 2007, with the
intent to defraud or mislead, Mr. Xu
caused introduction and delivery for
introduction into interstate commerce of
drugs that were misbranded, namely a
shipment containing blister strips of
ZYPREXA pills that were labeled in a
manner to falsely represent that these
blister strips contained genuine
ZYPREXA.
On or about February 20, 2007, with
the intent to defraud or mislead, Mr. Xu
caused the introduction and delivery for
introduction into interstate commerce of
drugs that were misbranded, namely a
shipment containing blister strips of
PLAVIX pills that were labeled in a
manner to falsely represent that these
blister strips contained genuine
PLAVIX.
On or about December 8, 2006, Mr. Xu
intentionally trafficked in goods,
namely pharmaceutical drugs, and
knowingly used a counterfeit mark, the
ZYPREXA trademark, on and in
connection with such goods.
As a result of his conviction, on
August 17, 2009, FDA sent Mr. Xu a
notice by certified mail proposing to
VerDate Nov<24>2008
16:26 Apr 07, 2010
Jkt 220001
permanently debar him from providing
services in any capacity to a person that
has an approved or pending drug
product application. The proposal was
based on a finding, under section
306(a)(2)(B) of the act that Kevin Xu was
convicted of a felony under Federal law
for conduct relating to the regulation of
a drug product under the act. The
proposal also offered Mr. Xu 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.
Xu failed to respond within the
timeframe prescribed by regulation and
has, therefore, waived his opportunity
for a hearing and any contentions
concerning his debarment (21 CFR part
12).
II. Findings and Order
Therefore, the Acting Director, Office
of Enforcement, Office of Regulatory
Affairs, under section 306(a)(2)(B) of the
act, under authority delegated to the
Acting Director (Staff Manual Guide
1410.35), finds that Kevin Xu has been
convicted of a felony under Federal law
for conduct relating to the regulation of
a drug product under the act.
As a result of the foregoing finding,
Mr. Xu is permanently debarred from
providing services in any capacity to a
person with an approved or pending
drug product application under sections
505, 512, or 802 of the act (21 U.S.C.
355, 360b, or 382), or under section 351
of the Public Health Service Act (42
U.S.C. 262), effective (see DATES) (see
section 306(c)(1)(B) and (c)(2)(A)(ii) and
section 201(dd) of the act (21 U.S.C.
321(dd))). Any person with an approved
or pending drug product application
who knowingly employs or retains as a
consultant or contractor, or otherwise
uses the services of Kevin Xu, in any
capacity during Mr. Xu’s debarment,
will be subject to civil money penalties
(section 307(a)(6) of the act (21 U.S.C.
335b(a)(6))). If Mr. Xu provides services
in any capacity to a person with an
approved or pending drug product
application during his period of
debarment he will be subject to civil
money penalties (section 307(a)(7) of the
act). In addition, FDA will not accept or
review any abbreviated new drug
applications submitted by or with the
assistance of Mr. Xu during his period
of debarment (section 306(c)(1)(B) of the
act).
Any application by Mr. Xu for special
termination of debarment under section
306(d)(4) of the act should be identified
with Docket No. FDA–2009–N–0286
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
and sent to the Division of Dockets
Management (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(j).
Publicly available submissions may
be seen in the Division of Dockets
Management between 9 a.m. and 4 p.m.,
Monday through Friday.
Dated: March 15, 2010.
Brenda Holman,
Acting Director, Office of Enforcement, Office
of Regulatory Affairs.
[FR Doc. 2010–8023 Filed 4–7–10; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–F–0103]
Nisso America, Inc.; Filing of Food
Additive Petition
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that Nisso America, Inc., has filed a
petition proposing that the food additive
regulations for hydroxypropyl cellulose
be amended by lowering the minimum
viscosity from 145 centipoises (cPs) to
10 cPs and to permit its use as a binder
in dietary supplements.
FOR FURTHER INFORMATION CONTACT:
Laura Dye, Center for Food Safety and
Applied Nutrition (HFS–265), Food and
Drug Administration, 5100 Paint Branch
Pkwy., College Park, MD 20740–3835,
301–436–1275.
SUPPLEMENTARY INFORMATION: Under the
Federal Food, Drug, and Cosmetic Act
(sec. 409(b)(5) (21 U.S.C. 348(b)(5))),
notice is given that a food additive
petition (FAP 0A4780) has been filed by
Nisso America, Inc., 45 Broadway, suite
2120, New York, NY 10006. The
petition proposes to amend the food
additive regulations in § 172.870
Hydroxypropyl cellulose (21 CFR
172.870) by lowering the minimum
permitted viscosity of hydroxypropyl
cellulose identified in paragraph (a)(1)
of this regulation from 145 cPs to 10 cPs
and to permit its use as a binder in
dietary supplements.
The agency has determined under 21
CFR 25.32(k) that this action is of a type
that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
E:\FR\FM\08APN1.SGM
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Agencies
[Federal Register Volume 75, Number 67 (Thursday, April 8, 2010)]
[Notices]
[Pages 17927-17928]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-8023]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA-2009-N-0286]
Kevin Xu: 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 (the act) permanently
debarring Kevin Xu from providing services in any capacity to a person
that has an approved or pending drug product application. FDA bases
this order on a finding that Mr. Xu was convicted of a felony under
Federal law for conduct relating to the regulation of a drug product
under the act. Mr. Xu was given notice of the proposed permanent
debarment and an opportunity to request a hearing within the timeframe
prescribed by regulation. As of September 23, 2009, Mr. Xu has failed
to respond. Mr. Xu's failure to respond constitutes a waiver of his
right to a hearing concerning this action.
DATES: This order is effective April 8, 2010.
ADDRESSES: Submit applications for special termination of debarment to
the Division of Dockets Management (HFA-305), Food and Drug
Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT: Kenny Shade, Division of Compliance
Policy (HFC-230), Office of Enforcement, Office of Regulatory Affairs,
Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857,
240-632-6844.
SUPPLEMENTARY INFORMATION:
I. Background
Section 306(a)(2)(B) of the act (21 U.S.C. 335a(a)(2)(B)) requires
debarment of an individual if FDA finds that the individual has been
convicted of a felony under Federal law for conduct otherwise relating
to the regulation of any drug product under the act.
On January 20, 2009, the U.S. District Court for the Southern
District of Texas entered judgment against Mr. Xu for one count of
participating in a conspiracy to traffic and attempt to traffic in
counterfeit goods, to cause the introduction and delivery for
introduction of misbranded prescription drugs into interstate commerce,
and to cause the counterfeiting of trademarks in violation of 18 U.S.C.
371, three counts of causing the introduction and delivery for
introduction of misbranded prescription drugs into interstate commerce
in violation of 21 U.S.C. 331(a) and 21 U.S.C. 333(a)(2), and one count
of trafficking in counterfeit goods
[[Page 17928]]
in violation of 18 U.S.C. 2320(a) and 18 U.S.C. 2320(a)(2).
FDA's finding that debarment is appropriate is based on the felony
convictions referenced herein for conduct relating to the regulation of
a drug product. The factual basis for those convictions is as follows:
From July 2006 until on or about July 2007, Mr. Xu did knowingly,
intentionally, and willfully conspire and agree with other persons to
import pharmaceutical drug products that bore the trademarks ZYPREXA,
TAMIFLU, CASODEX, PLAVIX, and ARICEPT without the authorization of the
manufacturer of these drugs, and then to resell these products to the
public.
On or about December 8, 2007, Mr. Xu used an Internet email address
to send an email listing the tracking numbers connected to the sale of
counterfeit pharmaceuticals. On or about April 9, 2007, Mr. Xu caused
coconspirators residing in the Republic of China to place in interstate
commerce for shipment to the United States various blister strips
containing counterfeit TAMIFLU, CASODEX, ZYPREXA, and PLAVIX.
On or about December 8, 2006, with the intent to defraud or
mislead, Mr. Xu caused the introduction and delivery for introduction
into interstate commerce of drugs that were misbranded, namely a
shipment containing blister strips of TAMIFLU capsules that were
labeled in a manner to falsely represent that these blister strips
contained genuine TAMIFLU.
On or about January 3, 2007, with the intent to defraud or mislead,
Mr. Xu caused introduction and delivery for introduction into
interstate commerce of drugs that were misbranded, namely a shipment
containing blister strips of ZYPREXA pills that were labeled in a
manner to falsely represent that these blister strips contained genuine
ZYPREXA.
On or about February 20, 2007, with the intent to defraud or
mislead, Mr. Xu caused the introduction and delivery for introduction
into interstate commerce of drugs that were misbranded, namely a
shipment containing blister strips of PLAVIX pills that were labeled in
a manner to falsely represent that these blister strips contained
genuine PLAVIX.
On or about December 8, 2006, Mr. Xu intentionally trafficked in
goods, namely pharmaceutical drugs, and knowingly used a counterfeit
mark, the ZYPREXA trademark, on and in connection with such goods.
As a result of his conviction, on August 17, 2009, FDA sent Mr. Xu
a notice by certified mail proposing to permanently debar him from
providing services in any capacity to a person that has an approved or
pending drug product application. The proposal was based on a finding,
under section 306(a)(2)(B) of the act that Kevin Xu was convicted of a
felony under Federal law for conduct relating to the regulation of a
drug product under the act. The proposal also offered Mr. Xu 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. Xu failed to respond within the timeframe prescribed by
regulation and has, therefore, waived his opportunity for a hearing and
any contentions concerning his debarment (21 CFR part 12).
II. Findings and Order
Therefore, the Acting Director, Office of Enforcement, Office of
Regulatory Affairs, under section 306(a)(2)(B) of the act, under
authority delegated to the Acting Director (Staff Manual Guide
1410.35), finds that Kevin Xu has been convicted of a felony under
Federal law for conduct relating to the regulation of a drug product
under the act.
As a result of the foregoing finding, Mr. Xu is permanently
debarred from providing services in any capacity to a person with an
approved or pending drug product application under sections 505, 512,
or 802 of the act (21 U.S.C. 355, 360b, or 382), or under section 351
of the Public Health Service Act (42 U.S.C. 262), effective (see DATES)
(see section 306(c)(1)(B) and (c)(2)(A)(ii) and section 201(dd) of the
act (21 U.S.C. 321(dd))). Any person with an approved or pending drug
product application who knowingly employs or retains as a consultant or
contractor, or otherwise uses the services of Kevin Xu, in any capacity
during Mr. Xu's debarment, will be subject to civil money penalties
(section 307(a)(6) of the act (21 U.S.C. 335b(a)(6))). If Mr. Xu
provides services in any capacity to a person with an approved or
pending drug product application during his period of debarment he will
be subject to civil money penalties (section 307(a)(7) of the act). In
addition, FDA will not accept or review any abbreviated new drug
applications submitted by or with the assistance of Mr. Xu during his
period of debarment (section 306(c)(1)(B) of the act).
Any application by Mr. Xu for special termination of debarment
under section 306(d)(4) of the act should be identified with Docket No.
FDA-2009-N-0286 and sent to the Division of Dockets Management (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(j).
Publicly available submissions may be seen in the Division of
Dockets Management between 9 a.m. and 4 p.m., Monday through Friday.
Dated: March 15, 2010.
Brenda Holman,
Acting Director, Office of Enforcement, Office of Regulatory Affairs.
[FR Doc. 2010-8023 Filed 4-7-10; 8:45 am]
BILLING CODE 4160-01-S