Submission for OMB Review; Comment Request, 19957-19958 [2015-08473]

Download as PDF asabaliauskas on DSK5VPTVN1PROD with NOTICES Federal Register / Vol. 80, No. 71 / Tuesday, April 14, 2015 / Notices www.regulations.gov/ #!docketDetail;D=APHIS–2015–0003 or in our reading room, which is located in room 1141 of the USDA South Building, 14th Street and Independence Avenue SW., Washington, DC. Normal reading room hours are 8 a.m. to 4:30 p.m., Monday through Friday, except holidays. To be sure someone is there to help you, please call (202) 799–7039 before coming. FOR FURTHER INFORMATION CONTACT: Dr. Donna Malloy, Operational Support Section, Center for Veterinary Biologics, Policy, Evaluation, and Licensing, VS, APHIS, 4700 River Road Unit 148, Riverdale, MD 20737–1231; phone (301) 851–3426, fax (301) 734–4314. For information regarding the environmental assessment or the risk analysis, or to request a copy of the environmental assessment (as well as the risk analysis with confidential business information removed), contact Dr. Patricia L. Foley, Risk Manager, Center for Veterinary Biologics, Policy, Evaluation, and Licensing, VS, APHIS, 1920 Dayton Avenue, P.O. Box 844, Ames, IA 50010; phone (515) 337–6100, fax (515) 337–6120. SUPPLEMENTARY INFORMATION: Under the Virus-Serum-Toxin Act (21 U.S.C. 151 et seq.), a veterinary biological product must be shown to be pure, safe, potent, and efficacious before a veterinary biological product license may be issued. A field test is generally necessary to satisfy prelicensing requirements for veterinary biological products. Prior to conducting a field test on an unlicensed product, an applicant must obtain approval from the Animal and Plant Health Inspection Service (APHIS), as well as obtain APHIS’ authorization to ship the product for field testing. To determine whether to authorize shipment and grant approval for the field testing of the unlicensed product referenced in this notice, APHIS considers the potential effects of this product on the safety of animals, public health, and the environment. Using the risk analysis and other relevant data, APHIS has prepared an environmental assessment (EA) concerning the field testing of the following unlicensed veterinary biological product: Requester: Merial, Inc. Product: Marek’s Disease Vaccine, Serotype 1, Live Virus. Possible Field Test Locations: Arkansas, Georgia, Kentucky, North Carolina, Tennessee, and Texas. The above-mentioned product is a live Marek’s Disease serotype 1 vaccine virus containing the long terminal repeat of the reticuloendotheliosis virus. VerDate Sep<11>2014 17:42 Apr 13, 2015 Jkt 235001 The attenuated vaccine is intended for use in healthy day-old chickens, as an aid in the prevention of Marek’s disease caused by very virulent Marek’s disease virus. The EA has been prepared in accordance with: (1) The National Environmental Policy Act of 1969 (NEPA), as amended (42 U.S.C. 4321 et seq.), (2) regulations of the Council on Environmental Quality for implementing the procedural provisions of NEPA (40 CFR parts 1500–1508), (3) USDA regulations implementing NEPA (7 CFR part 1b), and (4) APHIS’ NEPA Implementing Procedures (7 CFR part 372). Unless substantial issues with adverse environmental impacts are raised in response to this notice, APHIS intends to issue a finding of no significant impact (FONSI) based on the EA and authorize shipment of the above product for the initiation of field tests following the close of the comment period for this notice. Because the issues raised by field testing and by issuance of a license are identical, APHIS has concluded that the EA that is generated for field testing would also be applicable to the proposed licensing action. Provided that the field test data support the conclusions of the original EA and the issuance of a FONSI, APHIS does not intend to issue a separate EA and FONSI to support the issuance of the product license, and would determine that an environmental impact statement need not be prepared. APHIS intends to issue a veterinary biological product license for this vaccine following completion of the field test provided no adverse impacts on the human environment are identified and provided the product meets all other requirements for licensing. Authority: 21 U.S.C. 151–159. Done in Washington, DC, this 8th day of April 2015. Kevin Shea, Administrator, Animal and Plant Health Inspection Service. [FR Doc. 2015–08604 Filed 4–13–15; 8:45 am] BILLING CODE 3410–34–P DEPARTMENT OF COMMERCE Submission for OMB Review; Comment Request The Department of Commerce will submit to the Office of Management and Budget (OMB) for clearance the following proposal for collection of information under the provisions of the PO 00000 Frm 00003 Fmt 4703 Sfmt 4703 19957 Paperwork Reduction Act (44 U.S.C. chapter 35). Agency: U.S. Census Bureau. Title: Comparing Health Insurance Measurement Error (CHIME). OMB Control Number: 0607–XXXX. Form Number(s): No forms; respondent information collected by telephone interview. Type of Request: Regular submission. Number of Respondents: 5,000 Households. Average Hours per Response: 13 minutes. Burden Hours: 3,028 hours. Needs and Uses: The goal of the study is to assess measurement error in health coverage estimates that is ascribable to the questionnaire across the CPS and ACS health insurance modules using administrative records as a truth source. Both ‘‘absolute’’ reporting accuracy (the survey report compared to the administrative record data) and ‘‘relative’’ reporting accuracy (comparing absolute accuracy across questionnaire treatments) will be evaluated. The analysis will be used to understand the magnitude, direction and patterns of misreporting for three main purposes: (1) To provide Census program staff with empirical data to develop and refine edits and/or to include research notes for data users so they can make their own adjustments for misreporting; (2) to equip the wider research community with information that could serve as a guide for deciding which among the various surveys best suits their needs; and (3) to contribute to the general survey methods research literature on measurement error. Analysis will also inform reporting accuracy of health coverage related to the Affordable Care Act (ACA). Specifically, for coverage that is known to be obtained from the marketplace, we will explore whether respondents report that coverage, the source they cite (direct-purchase, government, etc.), and the accuracy with which they answer a question on subsidized premiums. Affected Public: Individuals or households. Frequency: One time. Respondent’s Obligation: Voluntary. Legal Authority: Title 13, United States Code, sections 141, 182 and 193. This information collection request may be viewed at www.reginfo.gov. Follow the instructions to view Department of Commerce collections currently under review by OMB. Written comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to OIRA_Submission@ omb.eop.gov or fax to (202)395–5806. E:\FR\FM\14APN1.SGM 14APN1 19958 Federal Register / Vol. 80, No. 71 / Tuesday, April 14, 2015 / Notices Dated: April 8, 2015. Glenna Mickelson, Management Analyst, Office of the Chief Information Officer. [FR Doc. 2015–08473 Filed 4–13–15; 8:45 am] BILLING CODE 3510–07–P DEPARTMENT OF COMMERCE Foreign-Trade Zones Board [B–86–2014] Production Activity Not Authorized; Foreign-Trade Zone 57—Charlotte, North Carolina; Gildan Yarns, LLC; (Cotton, Cotton/Polyester Yarns); Salisbury, North Carolina On December 8, 2014, the Charlotte Regional Partnership, grantee of FTZ 57, submitted a notification of proposed production activity to the Foreign-Trade Zones (FTZ) Board on behalf of Gildan Yarns, LLC, in Salisbury, North Carolina. The notification was processed in accordance with the regulations of the FTZ Board (15 CFR part 400), including notice in the Federal Register inviting public comment (79 FR 75532, 12–18– 2014). Pursuant to Section 400.37, the FTZ Board has determined that further review is warranted and has not authorized the proposed activity. If the applicant wishes to seek authorization for this activity, it will need to submit an application for production authority, pursuant to Section 400.23. Dated: April 8, 2015. Andrew McGilvray, Executive Secretary. [FR Doc. 2015–08592 Filed 4–13–15; 8:45 am] BILLING CODE 3510–DS–P DEPARTMENT OF COMMERCE Foreign-Trade Zones Board [B–20–2015] asabaliauskas on DSK5VPTVN1PROD with NOTICES Foreign-Trade Zone (FTZ) 50—Long Beach, California; Notification of Proposed Production Activity; Mercedes Benz USA, LLC; (Accessorizing Motor Vehicles); Long Beach, California The Port of Long Beach, grantee of FTZ 50, submitted a notification of proposed production activity to the FTZ Board on behalf of Mercedes Benz USA, LLC (MBUSA), located in Long Beach, California. The notification conforming to the requirements of the regulations of the FTZ Board (15 CFR 400.22) was received on March 24, 2015. The MBUSA facility is located within Site 41 of FTZ 50. The facility is used VerDate Sep<11>2014 17:42 Apr 13, 2015 Jkt 235001 for accessorizing passenger motor vehicles. Pursuant to 15 CFR 400.14(b), FTZ activity would be limited to the specific foreign-status materials and components and specific finished products described in the submitted notification (as described below) and subsequently authorized by the FTZ Board. Production under FTZ procedures could exempt MBUSA from customs duty payments on the foreign status components used in export production. On its domestic sales, MBUSA would be able to choose the duty rate during customs entry procedures that applies to passenger motor vehicles (duty rate¥2.5%) for the foreign status components noted below. Customs duties also could possibly be deferred or reduced on foreign status production equipment. The components sourced from abroad include: Plastic door sills and strips; wheel rim locks; metal door sills and strips; memory cards; navigation systems and related parts; entertainment systems; wiring sets and harnesses; storage compartments; spoilers; and, cup holders (duty rate ranges from free to 5%). Public comment is invited from interested parties. Submissions shall be addressed to the FTZ Board’s Executive Secretary at the address below. The closing period for their receipt is May 26, 2015. A copy of the notification will be available for public inspection at the Office of the Executive Secretary, Foreign-Trade Zones Board, Room 21013, U.S. Department of Commerce, 1401 Constitution Avenue NW., Washington, DC 20230–0002, and in the ‘‘Reading Room’’ section of the FTZ Board’s Web site, which is accessible via www.trade.gov/ftz. For further information, contact Pierre Duy at Pierre.Duy@trade.gov or (202) 482–1378. Dated: April 7, 2015. Andrew McGilvray, Executive Secretary. [FR Doc. 2015–08590 Filed 4–13–15; 8:45 am] BILLING CODE 3510–DS–P PO 00000 DEPARTMENT OF COMMERCE Foreign-Trade Zones Board [Order No. 1974] Reorganization of Foreign-Trade Zone 286; (Expansion of Service Area); Under Alternative Site Framework; Caledonia, Essex and Orleans Counties, Vermont Pursuant to its authority under the ForeignTrade Zones Act of June 18, 1934, as amended (19 U.S.C. 81a–81u), the ForeignTrade Zones Board (the Board) adopts the following Order: Whereas, the Board adopted the alternative site framework (ASF) (15 CFR Sec. 400.2(c)) as an option for the establishment or reorganization of zones; Whereas, the Northeastern Vermont Development Association, grantee of FTZ 286, submitted an application to the Board (FTZ Docket B–60–2014, docketed 08–27–2014) for authority to expand the service area of the zone to include Lamoille County, as described in the application, adjacent to the Derby Line Customs and Border Protection port of entry; Whereas, notice inviting public comment was given in the Federal Register (79 FR 52300, 09–03–14) and the application has been processed pursuant to the FTZ Act and the Board’s regulations; and, Whereas, the Board adopts the findings and recommendations of the examiner’s report, and finds that the requirements of the FTZ Act and the Board’s regulations are satisfied; Now, therefore, the Board hereby orders: The application to reorganize FTZ 286 to expand the service area under the ASF is approved, subject to the FTZ Act and the Board’s regulations, including Section 400.13, and to the Board’s standard 2,000-acre activation limit for the zone. Signed at Washington, DC this 3rd day of April 2015. Paul Piquado, Assistant Secretary of Commerce for Enforcement and Compliance, Alternate Chairman, Foreign-Trade Zones Board. ATTEST: lll Andrew McGilvray, Executive Secretary. [FR Doc. 2015–08584 Filed 4–13–15; 8:45 am] BILLING CODE 3510–DS–P Frm 00004 Fmt 4703 Sfmt 9990 E:\FR\FM\14APN1.SGM 14APN1

Agencies

[Federal Register Volume 80, Number 71 (Tuesday, April 14, 2015)]
[Notices]
[Pages 19957-19958]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-08473]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF COMMERCE


Submission for OMB Review; Comment Request

    The Department of Commerce will submit to the Office of Management 
and Budget (OMB) for clearance the following proposal for collection of 
information under the provisions of the Paperwork Reduction Act (44 
U.S.C. chapter 35).
    Agency: U.S. Census Bureau.
    Title: Comparing Health Insurance Measurement Error (CHIME).
    OMB Control Number: 0607-XXXX.
    Form Number(s): No forms; respondent information collected by 
telephone interview.
    Type of Request: Regular submission.
    Number of Respondents: 5,000 Households.
    Average Hours per Response: 13 minutes.
    Burden Hours: 3,028 hours.
    Needs and Uses: The goal of the study is to assess measurement 
error in health coverage estimates that is ascribable to the 
questionnaire across the CPS and ACS health insurance modules using 
administrative records as a truth source. Both ``absolute'' reporting 
accuracy (the survey report compared to the administrative record data) 
and ``relative'' reporting accuracy (comparing absolute accuracy across 
questionnaire treatments) will be evaluated. The analysis will be used 
to understand the magnitude, direction and patterns of misreporting for 
three main purposes: (1) To provide Census program staff with empirical 
data to develop and refine edits and/or to include research notes for 
data users so they can make their own adjustments for misreporting; (2) 
to equip the wider research community with information that could serve 
as a guide for deciding which among the various surveys best suits 
their needs; and (3) to contribute to the general survey methods 
research literature on measurement error. Analysis will also inform 
reporting accuracy of health coverage related to the Affordable Care 
Act (ACA). Specifically, for coverage that is known to be obtained from 
the marketplace, we will explore whether respondents report that 
coverage, the source they cite (direct-purchase, government, etc.), and 
the accuracy with which they answer a question on subsidized premiums.
    Affected Public: Individuals or households.
    Frequency: One time.
    Respondent's Obligation: Voluntary.
    Legal Authority: Title 13, United States Code, sections 141, 182 
and 193.
    This information collection request may be viewed at 
www.reginfo.gov. Follow the instructions to view Department of Commerce 
collections currently under review by OMB.
    Written comments and recommendations for the proposed information 
collection should be sent within 30 days of publication of this notice 
to OIRA_Submission@omb.eop.gov or fax to (202)395-5806.


[[Page 19958]]


    Dated: April 8, 2015.
Glenna Mickelson,
Management Analyst, Office of the Chief Information Officer.
[FR Doc. 2015-08473 Filed 4-13-15; 8:45 am]
 BILLING CODE 3510-07-P
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