Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act: Guidance for Industry and Food and Drug Administration Staff
Information
Type
Guidance
Regulated products
Medical Devices
Published
October 7, 2022
Last updated
October 17, 2022
Description
Guidance document providing information on postmarket surveillance under Section 522 of the Federal Food, Drug, and Cosmetic Act.
Tags
Organization
Country / Region
United States
License
Other (Public Domain)