Rule2022-02046

Laboratory Accreditation for Analyses of Foods; Correction

Primary source

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Published
February 2, 2022
Effective
February 1, 2022

Issuing agencies

Health and Human Services DepartmentFood and Drug Administration

Abstract

The Food and Drug Administration (FDA or we) is correcting a final rule that appeared in the Federal Register on December 3, 2021. The document amended our regulations to establish a program for the testing of food in certain circumstances by accredited laboratories, as required under the Federal Food, Drug, and Cosmetic Act. The final rule published with some editorial and inadvertent errors. This document corrects those errors.

Full Text

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<title>Federal Register, Volume 87 Issue 22 (Wednesday, February 2, 2022)</title>
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[Federal Register Volume 87, Number 22 (Wednesday, February 2, 2022)]
[Rules and Regulations]
[Page 5660]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2022-02046]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

21 CFR Part 1

[Docket No. FDA-2019-N-3325]
RIN 0910-AH31


Laboratory Accreditation for Analyses of Foods; Correction

AGENCY: Food and Drug Administration, Department of Health and Human 
Services (HHS).

ACTION: Final rule; correction.

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SUMMARY: The Food and Drug Administration (FDA or we) is correcting a 
final rule that appeared in the Federal Register on December 3, 2021. 
The document amended our regulations to establish a program for the 
testing of food in certain circumstances by accredited laboratories, as 
required under the Federal Food, Drug, and Cosmetic Act. The final rule 
published with some editorial and inadvertent errors. This document 
corrects those errors.

DATES: Effective February 1, 2022.

FOR FURTHER INFORMATION CONTACT: Stacie Hammack, Food and Feed 
Laboratory Operations, Office of Regulatory Affairs, Food and Drug 
Administration, 60 8th Street NE, Atlanta, GA 30309, 301-796-5817, 
<a href="/cdn-cgi/l/email-protection#ebb89f8a88828ec5a38a86868a8880ab8d8f8ac5838398c58c849d"><span class="__cf_email__" data-cfemail="316245505258541f79505c5c50525a715755501f5959421f565e47">[email&#160;protected]</span></a>.

SUPPLEMENTARY INFORMATION: In the Federal Register of Friday, December 
3, 2021, in FR Doc. 2021-25716, appearing on page 68728, the following 
corrections are made:

PART 1--GENERAL ENFORCEMENT REGULATIONS

Subpart R [Corrected]

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1. On page 68817, in the second column, in part 1, subpart R, the table 
of contents entry for Sec.  1.1124 is corrected to read ``What are the 
records requirements for a recognized accreditation body?''.

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2. On page 68823, in the first column, in part 1, subpart R, the 
undesignated heading between Sec. Sec.  1.1125 and 1.1130 is corrected 
to read ``FDA Oversight of Recognized Accreditation Bodies''.


Sec.  1.1131  [Corrected]

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3. On page 68823, in the second column, Sec.  1.1131(a)(2) is corrected 
by removing ``ISO/IEC 17011:2017 section 9.5'' and adding ``ISO/IEC 
17011:2017(E) section 9.5'' in its place.

    Dated: January 25, 2022.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2022-02046 Filed 2-1-22; 8:45 am]
BILLING CODE 4164-01-P


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Indexed from Federal Register on February 2, 2022.

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