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# Info Collection Extension on Device Quality System
- URL: https://www.fdaweb.com/info-collection-extension-on-device-quality-system/
- Published: 2019-11-14T12:00:00.000Z
- Updated: 2026-09-14T15:53:10.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5145505

Federal Register notice: FDA has submitted to OMB an information collection extension for “Medical Devices: Current Good Manufacturing Practice Quality System Regulation — 21 CFR Part 820” (OMB Control Number 0910-0073). This regulation includes requirements for purchasing and service controls, clarifies recordkeeping requirements for device failure and complaint investigations, clarifies requirements for verifying/validating production processes and process or product changes, and clarifies requirements for product acceptance activities, quality data evaluations, and corrections of nonconforming product/quality problems. To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2019-24805.pdf?ref=fdaweb.com).