# Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act:  Guidance for Industry and Food and Drug Administration Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/postmarket-surveillance-under-section-522-of-the-federal-food-drug-and-cosmetic-act-guidance-for-industry-and-food-and-drug-administration-staff/f631d61d-d1a4-451d-84c0-b22c554e8218

> FDA guidance document: Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act:  Guidance for Industry and Food and Drug Administration Staff. Issue date: October 07, 2022. Get complete insights and analysis.

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## Details

- Title: Postmarket Surveillance Under Section 522 of the Federal Food, Drug, and Cosmetic Act:  Guidance for Industry and Food and Drug Administration Staff
- Communication Type: Guidance Document
- Product Type: devices
- Office Name: Center for Devices and Radiological Health
- Office URL: /offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
- Issue Date: 2022-10-07
- Last Changed: 2022-10-17
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2011-D-0514">FDA-2011-D-0514</a>

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