# Medical Devices; Quality System Regulation Amendments; Correction
> **Food and Drug Administration** · Final rule; correction. · Published 2024-10-15 · Effective 2026-02-02 · 89 FR 82945
## Document
- **Document number:** 2024-23701
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 89 FR 82945
- **CFR reference:** 21 CFR 820
- **Publication date:** 2024-10-15
- **Effective date:** 2026-02-02
- **HHS docket:** Docket No. FDA-2021-N-0507
## Abstract

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.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2024/10/15/2024-23701/medical-devices-quality-system-regulation-amendments-correction)
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