Manufacturer of Controlled Substances; Notice of Application, 31638-31639 [2011-13487]
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Federal Register / Vol. 76, No. 105 / Wednesday, June 1, 2011 / Notices
completed fiscal year (identify the date
on which your fiscal year ends).
(10) If you are a U.S. importer or a
trade/business association of U.S.
importers of the Subject Merchandise
from the Subject Country, provide the
following information on your firm’s(s’)
operations on that product during
calendar year 2010 (report quantity data
in metric tons and value data in U.S.
dollars). If you are a trade/business
association, provide the information, on
an aggregate basis, for the firms which
are members of your association.
(a) The quantity and value (landed,
duty-paid but not including
antidumping duties) of U.S. imports
and, if known, an estimate of the
percentage of total U.S. imports of
Subject Merchandise from the Subject
Country accounted for by your firm’s(s’)
imports;
(b) The quantity and value (f.o.b. U.S.
port, including antidumping duties) of
U.S. commercial shipments of Subject
Merchandise imported from the Subject
Country; and
(c) The quantity and value (f.o.b. U.S.
port, including antidumping duties) of
U.S. internal consumption/company
transfers of Subject Merchandise
imported from the Subject Country.
(11) If you are a producer, an exporter,
or a trade/business association of
producers or exporters of the Subject
Merchandise in the Subject Country,
provide the following information on
your firm’s(s’) operations on that
product during calendar year 2010
(report quantity data in metric tons and
value data in U.S. dollars, landed and
duty-paid at the U.S. port but not
including antidumping duties). If you
are a trade/business association, provide
the information, on an aggregate basis,
for the firms which are members of your
association.
(a) Production (quantity) and, if
known, an estimate of the percentage of
total production of Subject Merchandise
in the Subject Country accounted for by
your firm’s(s’) production;
(b) Capacity (quantity) of your firm to
produce the Subject Merchandise in the
Subject Country (i.e., the level of
production that your establishment(s)
could reasonably have expected to
attain during the year, assuming normal
operating conditions (using equipment
and machinery in place and ready to
operate), normal operating levels (hours
per week/weeks per year), time for
downtime, maintenance, repair, and
cleanup, and a typical or representative
product mix); and
(c) The quantity and value of your
firm’s(s’) exports to the United States of
Subject Merchandise and, if known, an
estimate of the percentage of total
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18:48 May 31, 2011
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exports to the United States of Subject
Merchandise from the Subject Country
accounted for by your firm’s(s’) exports.
(12) Identify significant changes, if
any, in the supply and demand
conditions or business cycle for the
Domestic Like Product that have
occurred in the United States or in the
market for the Subject Merchandise in
the Subject Country after 2005, and
significant changes, if any, that are
likely to occur within a reasonably
foreseeable time. Supply conditions to
consider include technology;
production methods; development
efforts; ability to increase production
(including the shift of production
facilities used for other products and the
use, cost, or availability of major inputs
into production); and factors related to
the ability to shift supply among
different national markets (including
barriers to importation in foreign
markets or changes in market demand
abroad). Demand conditions to consider
include end uses and applications; the
existence and availability of substitute
products; and the level of competition
among the Domestic Like Product
produced in the United States, Subject
Merchandise produced in the Subject
Country, and such merchandise from
other countries.
(13) (OPTIONAL) A statement of
whether you agree with the above
definitions of the Domestic Like Product
and Domestic Industry; if you disagree
with either or both of these definitions,
please explain why and provide
alternative definitions.
Federal Trade Commission disclosing
changes in its membership and its
nature and objectives. The notifications
were filed for the purpose of extending
the Act’s provisions limiting the
recovery of antitrust plaintiffs to actual
damages under specified circumstances.
Specifically, Toyota Motor Corporation,
Aichi, Japan, has withdrawn as a party
to this venture. The change in its nature
and objectives is that the members of
GCEP have amended the agreement
between them to extend the termination
of GCEP, which currently will terminate
August 31, 2013.
No other changes have been made in
either the membership or planned
activity of the group research project.
Membership in this group research
project remains open, and GCEP intends
to file additional written notifications
disclosing all changes in membership.
On March 12, 2003, GCEP filed its
original notification pursuant to Section
6(a) of the Act. The Department of
Justice published a notice in the Federal
Register pursuant to Section 6(b) of the
Act on April 4, 2003 (68 FR 16552).
The last notification was filed with
the Department on February 26, 2009. A
notice was published in the Federal
Register pursuant to Section 6(b) of the
Act April 3, 2009 (74 FR 15303).
Patricia A. Brink,
Director of Civil Enforcement, Antitrust
Division.
[FR Doc. 2011–13306 Filed 5–31–11; 8:45 am]
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Authority: This review is being conducted
under authority of title VII of the Tariff Act
of 1930; this notice is published pursuant to
section 207.61 of the Commission’s rules.
DEPARTMENT OF JUSTICE
By order of the Commission.
Issued: May 25, 2011.
James R. Holbein,
Secretary to the Commission.
Manufacturer of Controlled
Substances; Notice of Application
[FR Doc. 2011–13448 Filed 5–31–11; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
Antitrust Division
Notice Pursuant to the National
Cooperative Research and Production
Act of 1993—Global Climate and
Energy Project
Notice is hereby given that, on April
8, 2011, pursuant to Section 6(a) of the
National Cooperative Research and
Production Act of 1993, 15 U.S.C. 4301
et seq. (‘‘the Act’’), Global Climate and
Energy Project (‘‘GCEP’’) has filed
written notifications simultaneously
with the Attorney General and the
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Drug Enforcement Administration
Pursuant to § 1301.33(a), Title 21 of
the Code of Federal Regulations (CFR),
this is notice that on February 15, 2011,
Wildlife Laboratories Inc., 1401 Duff
Drive, Suite 400, Fort Collins, Colorado
80524, made application by renewal to
the Drug Enforcement Administration
(DEA) to be registered as a bulk
manufacturer of Carfentanil (9743), a
basic class of controlled substance listed
in schedule II.
The company plans to manufacture
the above listed controlled substance for
sale to veterinary pharmacies, zoos, and
for other animal and wildlife
applications.
Any other such applicant, and any
person who is presently registered with
DEA to manufacture such substance,
may file comments or objections to the
issuance of the proposed registration
pursuant to 21 CFR 1301.33(a).
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Federal Register / Vol. 76, No. 105 / Wednesday, June 1, 2011 / Notices
Any such comments or objections
should be addressed, in quintuplicate,
to the Drug Enforcement
Administration, Office of Diversion
Control, Federal Register Representative
(ODL), 8701 Morrissette Drive,
Springfield, Virginia 22152; and must be
filed no later than August 1, 2011.
Dated: May 25, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of
Diversion Control, Drug Enforcement
Administration.
[FR Doc. 2011–13487 Filed 5–31–11; 8:45 am]
BILLING CODE 4410–09–P
the public which raised technical and
non-technical issues and questions.
Following a thorough review of all
public comments and environmental
documentation amassed in support of
the proposed action, the BOP
determined that it was appropriate and
in the best interests of the public to
prepare a new EA. The new EA
incorporated additional information
prepared in response to public
comments. The new EA also provided
the most current information available
regarding the alternative facilities as
well as the BOP’s Preferred Alternative.
Project Information
DEPARTMENT OF JUSTICE
Federal Bureau of Prisons
Notice of the Availability of the Finding
of No Significant Impact Concerning a
Proposal To Award a Contract to
House Federal, Low-Security, Criminal
Aliens in a Contractor-Owned/
Contractor-Operated Correctional
Facility
U.S. Department of Justice,
Federal Bureau of Prisons.
ACTION: Finding of No Significant
Impact.
AGENCY:
The U.S. Department of
Justice, Federal Bureau of Prisons (BOP)
announces the availability of the
Finding of No Significant Impact
(FONSI) concerning the Environmental
Assessment (EA) for the proposal to
award one or more contracts to house
900 to approximately 3,000 federal, lowsecurity, adult male, non-U.S. citizen,
criminal aliens within one or more
existing contractor-owned and operated
correctional facilities.
SUMMARY:
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Background Information
Pursuant to Section 102, 42 U.S.C.
4332, of the National Environmental
Policy Act (NEPA) of 1969, as amended
and the Council on Environmental
Quality Regulations (40 CFR parts 1500–
1508), the BOP published an EA
concerning a proposal to award one or
more contracts to house 900 to
approximately 3,000 Federal, lowsecurity, adult male, non-U.S. citizen,
criminal aliens within one or more
existing contractor-owned and operated
correctional facilities.
The 30-day public comment period
began on January 28, 2011 and was
extended by 10 days at the request of a
member of the public in order to submit
comments to the BOP concerning the
EA. By March 9, 2011, the BOP received
comment letters from several
government agencies and a member of
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18:48 May 31, 2011
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Under the proposed action, the
contractor(s) selected to house the
approximately 3,000 Federal, lowsecurity, adult male, criminal aliens
would be responsible for ensuring that
the correctional facility(s) is operated in
a manner consistent with the mission of
the BOP and state and federal laws and
regulations. It is anticipated that the
BOP will predominantly assign Federal,
low-security, adult male, criminal aliens
(comprised primarily of persons with a
year or less remaining to serve) to the
selected facility. However, the BOP may
designate any inmate within its custody
utilizing the same designation criteria as
used at other BOP facilities. All inmate
services and programs would be
developed and implemented to comply
with the BOP’s contract requirements
and all applicable federal, state and
local laws and regulations.
Following publication of the
solicitation for the Short Term
Sentences procurement, the BOP
received responses from contractors
representing nine alternative facilities.
Of the nine alternative locations, six
were either withdrawn by contractor(s)
or eliminated from consideration by the
BOP on the basis of non-environmental
criteria. Three existing correctional
facilities, located in Oklahoma and
Texas, were considered worthy of
further consideration. Possible use of
each of three existing facilities, in
addition to the No Action alternative,
were evaluated in an EA prepared by
the BOP. The BOP would select one or
more contractors for contract award
from among the three offerors:
—Diamondback Correctional Center,
Watonga, Oklahoma.
—Great Plains Correctional Facility,
Hinton, Oklahoma.
—Willacy County Processing Center,
Raymondville, Texas.
No other facilities were under
consideration by the BOP. The BOP
reserves the right to make multiple
awards. In the event it is in the
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Government’s best interest, the BOP
may make up to two (based on
proposals received) contract awards as
long as the total quantity is within the
scope of approximately 3,000 beds.
The BOP issued the EA on May 2,
2011, with publication of the Notice of
Availability (NOA) in newspapers
serving the area surrounding each of the
alternative locations. The NOA included
information concerning the 30-day
public comment period which began on
May 2, 2011, and ended on May 31,
2011. The BOP also distributed copies
of the EA to federal agencies, state and
local governments, elected officials,
interested organizations, public libraries
and individuals.
Availability of Finding of No
Significant Impact
The FONSI is available upon request.
To request a copy of the FONSI, please
contact: Richard A. Cohn, Chief, or Issac
J. Gaston, Site Selection Specialist,
Capacity Planning and Site Selection
Branch, Federal Bureau of Prisons, 320
First Street, NW., Washington, DC
20534 Tel: 202–514–6470/Fax: 202–
616–6024/E-mail: racohn@bop.gov or
IGaston@bop.gov
FOR FURTHER INFORMATION CONTACT:
Richard A. Cohn, or Issac J. Gaston,
Federal Bureau of Prisons.
Dated: May 24, 2011,
Richard A. Cohn,
Chief, Capacity Planning and Site Selection
Branch.
[FR Doc. 2011–13486 Filed 5–31–11; 8:45 am]
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DEPARTMENT OF LABOR
Comment Request for Information
Collection for Enhanced Transitional
Jobs Demonstration, New Collection
Employment and Training
Administration, Labor.
ACTION: Notice.
AGENCY:
The Department of Labor, as
part of its continuing effort to reduce
paperwork and respondent burden
conducts a preclearance consultation
program to provide the general public
and Federal agencies with an
opportunity to comment on proposed
and/or continuing collections of
information in accordance with the
Paperwork Reduction Act of 1995
(PRA95) [44 U.S.C. 3506(c)(2)(A)]. This
program helps to ensure that requested
data can be provided in the desired
format, reporting burden (time and
financial resources) is minimized,
collection instruments are clearly
SUMMARY:
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Agencies
[Federal Register Volume 76, Number 105 (Wednesday, June 1, 2011)]
[Notices]
[Pages 31638-31639]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-13487]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
Manufacturer of Controlled Substances; Notice of Application
Pursuant to Sec. 1301.33(a), Title 21 of the Code of Federal
Regulations (CFR), this is notice that on February 15, 2011, Wildlife
Laboratories Inc., 1401 Duff Drive, Suite 400, Fort Collins, Colorado
80524, made application by renewal to the Drug Enforcement
Administration (DEA) to be registered as a bulk manufacturer of
Carfentanil (9743), a basic class of controlled substance listed in
schedule II.
The company plans to manufacture the above listed controlled
substance for sale to veterinary pharmacies, zoos, and for other animal
and wildlife applications.
Any other such applicant, and any person who is presently
registered with DEA to manufacture such substance, may file comments or
objections to the issuance of the proposed registration pursuant to 21
CFR 1301.33(a).
[[Page 31639]]
Any such comments or objections should be addressed, in
quintuplicate, to the Drug Enforcement Administration, Office of
Diversion Control, Federal Register Representative (ODL), 8701
Morrissette Drive, Springfield, Virginia 22152; and must be filed no
later than August 1, 2011.
Dated: May 25, 2011.
Joseph T. Rannazzisi,
Deputy Assistant Administrator, Office of Diversion Control, Drug
Enforcement Administration.
[FR Doc. 2011-13487 Filed 5-31-11; 8:45 am]
BILLING CODE 4410-09-P