The Food and Drug Administration (FDA or Agency) is correcting a final rule that appeared in the Federal Register on February 2, 2024. In that final rule, FDA amended the device current good manufacturing practice (CGMP) requirements of the Quality System (QS) regulation to harmonize and modernize the device CGMP. FDA is correcting an editorial error that inadvertently omitted a definition in the codified of the final rule. This action is editorial in nature and is intended to ensure the accuracy and clarity of the Agency's regulations.
This is a final rule published in the Federal Register by Health and Human Services Department, Food and Drug Administration. Final rules have completed the public comment process and establish legally binding requirements.
Yes. This rule has been finalized. It has completed the notice-and-comment process required under the Administrative Procedure Act.
Final rule; correction.
This document has been effective since February 2, 2026.
This final rule likely has a preceding Notice of Proposed Rulemaking (NPRM), but we haven't linked it yet.
Our system will automatically fetch and link related NPRMs as they're discovered.
| Document Number | 2024-23701 |
| FR Citation | 89 FR 82945 |
| Type | Final Rule |
| Published | Oct 15, 2024 |
| Effective Date | Feb 2, 2026 |
| RIN | 0910-AH99 |
| Docket ID | Docket No. FDA-2021-N-0507 |
| Pages | 82945–82945 (1 pages) |
| Text Fetched | Yes |
| Part | Name | Agency |
|---|---|---|
| 21 CFR 820 | Quality System Regulation... | - |
| Type | Proposed | Final | Method | Conf |
|---|---|---|---|---|
| No paired documents | ||||
| Doc # | Type | Title | Published |
|---|---|---|---|
| 2024-01709 | Final Rule | Medical Devices; Quality System Regulati... | Feb 2, 2024 |
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