Federal Register - June 1, 2021
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Source: Federal Register
29272
Federal Register / Vol. 86, No. 103 / Tuesday, June 1, 2021 / Notices
jbell on DSKJLSW7X2PROD with NOTICES
6791630, Formerly: GammaDynacare Medical Laboratories ElSohly Laboratories, Inc., 5 Industrial Park Drive, Oxford, MS 38655, 662
2362609
Laboratory Corporation of America Holdings, 7207 N Gessner Road, Houston, TX 77040, 7138568288/
8008002387
Laboratory Corporation of America Holdings, 69 First Ave., Raritan, NJ
08869, 9085262400/8004374986, Formerly: Roche Biomedical Laboratories, Inc.
Laboratory Corporation of America Holdings, 1904 TW Alexander Drive, Research Triangle Park, NC 27709, 9195726900/8008333984, Formerly: LabCorp Occupational Testing Services, Inc., CompuChem Laboratories, Inc.; CompuChem Laboratories, Inc., A Subsidiary of Roche Biomedical Laboratory; Roche CompuChem Laboratories, Inc., A
Member of the Roche Group Laboratory Corporation of America Holdings, 1120 Main Street, Southaven, MS 38671, 8668278042/
8002336339, Formerly: LabCorp Occupational Testing Services, Inc.;
MedExpress/National Laboratory Center LabOne, Inc. d/b/a Quest Diagnostics, 10101 Renner Blvd., Lenexa, KS
66219, 9138883927/8008738845, Formerly: Quest Diagnostics Incorporated; LabOne, Inc.; Center for Laboratory Services, a Division of LabOne, Inc.
Legacy Laboratory Services Toxicology, 1225 NE 2nd Ave., Portland, OR
97232, 5034135295/8009505295
MedTox Laboratories, Inc., 402 W
County Road D, St. Paul, MN 55112, 6516367466/8008323244
Minneapolis Veterans Affairs Medical Center, Forensic Toxicology Laboratory, 1 Veterans Drive, accredited to conduct forensic urine drug testing as required by U.S. Department of Transportation DOT regulations. As of that date, the certification of those accredited Canadian laboratories will continue under DOT authority. The responsibility for conducting quarterly performance testing plus periodic on-site inspections of those LAPSAaccredited laboratories was transferred to the U.S.
HHS, with the HHS NLCP contractor continuing to have an active role in the performance testing and laboratory inspection processes. Other Canadian laboratories wishing to be considered for the NLCP
may apply directly to the NLCP contractor just as U.S. laboratories do.
Upon finding a Canadian laboratory to be qualified, HHS will recommend that DOT certify the laboratory Federal Register, July 16, 1996 as meeting the minimum standards of the Mandatory Guidelines published in the Federal Register on January 23, 2017 82 FR 7920. After receiving DOT
certification, the laboratory will be included in the monthly list of HHS-certified laboratories and participate in the NLCP certification maintenance program.
VerDate Sep<11>2014
18:20 May 28, 2021
Jkt 253001
Minneapolis, MN 55417, 612725
2088. Testing for Veterans Affairs VA Employees Only Pacific Toxicology Laboratories, 9348
DeSoto Ave., Chatsworth, CA 91311, 8003286942, Formerly: Centinela Hospital Airport Toxicology Laboratory Phamatech, Inc., 15175 Innovation Drive, San Diego, CA 92128, 888
6355840
Quest Diagnostics Incorporated, 400
Egypt Road, Norristown, PA 19403, 6106314600/8776422216, Formerly: SmithKline Beecham Clinical Laboratories; SmithKline BioScience Laboratories Redwood Toxicology Laboratory, 3700
Westwind Blvd., Santa Rosa, CA
95403, 8002552159
U.S. Army Forensic Toxicology Drug Testing Laboratory, 2490 Wilson St., Fort George G. Meade, MD 20755
5235, 3016777085, Testing for Department of Defense DoD
Employees Only Anastasia Marie Donovan, Policy Analyst.
FR Doc. 202111486 Filed 52821; 8:45 am BILLING CODE 416220P
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection 16510008
Application for Identification Card U.S. Customs and Border Protection CBP, Department of Homeland Security.
ACTION: 30-Day notice and request for comments; extension of an existing collection of information.
AGENCY:
The Department of Homeland Security, U.S. Customs and Border Protection will be submitting the following information collection request to the Office of Management and Budget OMB for review and approval in accordance with the Paperwork Reduction Act of 1995 PRA. The information collection is published in the Federal Register to obtain comments from the public and affected agencies.
DATES: Comments are encouraged and must be submitted no later than July 1, 2021 to be assured of consideration.
ADDRESSES: Written comments and/or suggestions regarding the items contained in this notice should be sent within 30 days of publication of this notice to www.reginfo.gov/public/do/
PRAMain. Find this particular information collection, OMB Control SUMMARY:
PO 00000
Frm 00040
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Number 16510008, by selecting Currently under 30-day ReviewOpen for Public Comments or by using the search function.
FOR FURTHER INFORMATION CONTACT:
Requests for additional PRA information should be directed to Seth Renkema, Chief, Economic Impact Analysis Branch, U.S. Customs and Border Protection, Office of Trade, Regulations and Rulings, 90 K Street NE, 10th Floor, Washington, DC 202291177, Telephone number 2023250056 or via email CBP_PRA@cbp.dhs.gov. Please note that the contact information provided here is solely for questions regarding this notice. Individuals seeking information about other CBP
programs should contact the CBP
National Customer Service Center at 8772275511, TTY 18008778339, or CBP website at https www.cbp .gov/.
CBP
invites the general public and other Federal agencies to comment on the proposed and/or continuing information collections pursuant to the Paperwork Reduction Act of 1995 44 U.S.C. 3501
et seq.. This proposed information collection was previously published in the Federal Register 86 FR 16605 on March 30, 2021, allowing for a 60-day comment period. This notice allows for an additional 30 days for public comments. This process is conducted in accordance with 5 CFR 1320.8. Written comments and suggestions from the public and affected agencies should address one or more of the following four points: 1 Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; 2 the accuracy of the agencys estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3
suggestions to enhance the quality, utility, and clarity of the information to be collected; and 4 suggestions to minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submission of responses. The comments that are submitted will be summarized and included in the request for approval. All comments will become a matter of public record.
SUPPLEMENTARY INFORMATION:
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