Rules of Practice, 45063 [C1-2023-12630]

Download as PDF Federal Register / Vol. 88, No. 134 / Friday, July 14, 2023 / Rules and Regulations Bend, OR, KBDN, VOR RWY 16, Amdt 11 Florence, SC, KFLO, ILS OR LOC RWY 9, Amdt 13 Florence, SC, KFLO, RNAV (GPS) RWY 1, Amdt 1 Florence, SC, KFLO, RNAV (GPS) RWY 9, Amdt 1 Florence, SC, KFLO, RNAV (GPS) RWY 19, Amdt 1 Florence, SC, KFLO, RNAV (GPS) RWY 27, Amdt 1 Sumter, SC, KSMS, ILS OR LOC RWY 23, Amdt 2 Sumter, SC, KSMS, Takeoff Minimums and Obstacle DP, Amdt 1A Seattle, WA, KBFI, RNAV (GPS) Y RWY 14R, Orig Seattle, WA, KBFI, RNAV (GPS) Y RWY 14R, Amdt 1A, CANCELED Seattle, WA, KBFI, RNAV (GPS) Y RWY 32L, Orig Seattle, WA, KBFI, RNAV (RNP) Z RWY 14R, Orig Seattle, WA, KBFI, RNAV (RNP) Z RWY 14R, Amdt 1A, CANCELED Seattle, WA, KBFI, RNAV (RNP) Z RWY 32L, Orig Rescinded: On June 21, 2023 (88 FR 40081), the FAA published an Amendment in Docket No. 31490, Amdt No. 4063, to part 97 of the Federal Aviation Regulations under §§ 97.23, 97.29, and 97.33. The following entries for Northway, AK, San Francisco, CA, and Cross Keys, NJ, effective August 10, 2023, are hereby rescinded in their entirety: Northway, AK, PAOR, RNAV (GPS) RWY 6, Amdt 1 Northway, AK, PAOR, RNAV (GPS) RWY 24, Amdt 2 San Francisco, CA, KSFO, GLS RWY 19L, Amdt 1 San Francisco, CA, KSFO, GLS RWY 19R, Amdt 1 Cross Keys, NJ, 17N, VOR OR GPS RWY 9, Amdt 6B, CANCELED [FR Doc. 2023–14932 Filed 7–13–23; 8:45 am] BILLING CODE 4910–13–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2023–N–0963] Nomenclature Change for Dockets Management; Technical Amendment Food and Drug Administration, Department of Health and Human Services (HHS). ACTION: Final rule; technical amendment. AGENCY: The Food and Drug Administration (FDA) is amending its regulations to reflect a change in the name of Division of Dockets Management to Dockets Management Staff and information regarding copies. This action is editorial in nature and is intended to improve the accuracy of the Agency’s regulations. DATES: This rule is effective July 14, 2023. FOR FURTHER INFORMATION CONTACT: Karen Malvin, Dockets Management Staff, Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240–402–7500. SUPPLEMENTARY INFORMATION: FDA is amending 21 CFR chapter I to update Dockets Management Staff’s name change and information regarding copies. Publication of this document constitutes final action on the changes under the Administrative Procedure Act (5 U.S.C. 553). FDA has determined that notice and public comment are unnecessary because this amendment to the regulations provides only a technical change to update the organizational information for Dockets Management Staff. SUMMARY: 21 CFR Part 3 Administrative practice and procedure, Biologics, Drugs, Medical devices. 16 CFR Parts 0, 1, 2, 3 and 4 lotter on DSK11XQN23PROD with RULES1 Rules of Practice In rule document 2023–12630 beginning on page 42872 in the issue of Wednesday, July 5, 2023, make the following corrections: On page 42872, in the third column, under DATES, in the first and fourth lines ‘‘June 5, 2023’’ should read ‘‘July 5, 2023’’. [FR Doc. C1–2023–12630 Filed 7–13–23; 8:45 am] BILLING CODE 0099–10–D VerDate Sep<11>2014 15:54 Jul 13, 2023 Jkt 259001 21 CFR Parts 12, 13, and 15 Administrative practice and procedure. 21 CFR Part 14 21 CFR Chapter I List of Subjects FEDERAL TRADE COMMISSION 45063 21 CFR Part 5 Authority delegations (Government agencies), Imports, Organization and functions (Government agencies). Administrative practice and procedure, Advisory committees, Color additives, Drugs, Radiation protection. 21 CFR Part 17 Administrative practice and procedure, Penalties. 21 CFR Part 20 Confidential business information, Courts, Freedom of information, Government employees. 21 CFR Part 25 Environmental impact statements, Foreign relations, Reporting and recordkeeping requirements. 21 CFR Part 60 Administrative practice and procedure, Drugs, Food additives, Inventions and patents, Medical devices, Reporting and recordkeeping requirements. 21 CFR Part 100 Administrative practice and procedure, Food labeling, Food packaging, Foods, Intergovernmental relations. 21 CFR Part 101 Food labeling, Nutrition, Reporting and recordkeeping requirements. 21 CFR Part 109 Food packaging, Foods, Polychlorinated biphenyls (PCBs). 21 CFR Part 165 Beverages, Bottled water, Food grades and standards. 21 CFR Part 170 Administrative practice and procedure, Food additives, Reporting and recordkeeping requirements. 21 CFR Part 184 Food additives. 21 CFR Part 201 Drugs, Labeling, Reporting and recordkeeping requirements. 21 CFR Part 7 Administrative practice and procedure, Consumer protection, Reporting and recordkeeping requirements. 21 CFR Part 312 21 CFR Part 10 Administrative practice and procedure, News media. 21 CFR Part 314 PO 00000 Frm 00009 Fmt 4700 Sfmt 4700 Drugs, Exports, Imports, Investigations, Labeling, Medical research, Reporting and recordkeeping requirements, Safety. Administrative practice and procedure, Confidential business E:\FR\FM\14JYR1.SGM 14JYR1

Agencies

[Federal Register Volume 88, Number 134 (Friday, July 14, 2023)]
[Rules and Regulations]
[Page 45063]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: C1-2023-12630]


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FEDERAL TRADE COMMISSION

16 CFR Parts 0, 1, 2, 3 and 4


Rules of Practice

    In rule document 2023-12630 beginning on page 42872 in the issue of 
Wednesday, July 5, 2023, make the following corrections:
    On page 42872, in the third column, under DATES, in the first and 
fourth lines ``June 5, 2023'' should read ``July 5, 2023''.

[FR Doc. C1-2023-12630 Filed 7-13-23; 8:45 am]
BILLING CODE 0099-10-D
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