1. Postmarket surveillance under section 522 of the Federal Food, Drug, and Cosmetic Act: guidance for industry and Food and Drug Administration staff Publication: [Silver Spring, MD] : Center for Devices and Radiological Health, October 7, 2022 Subject(s): Device Approval -- legislation & jurisprudenceGovernment RegulationProduct Surveillance, PostmarketingUnited StatesUnited States. Food and Drug Administration
