# Initiation of Voluntary Recalls Under 21 CFR Part 7, Subpart C:  Guidance for Industry and FDA Staff - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/initiation-of-voluntary-recalls-under-21-cfr-part-7-subpart-c-guidance-for-industry-and-fda-staff/b9272870-cad6-4e91-9fc0-e325feb24e43

> FDA guidance document: Initiation of Voluntary Recalls Under 21 CFR Part 7, Subpart C:  Guidance for Industry and FDA Staff. Issue date: March 04, 2022. Get complete insights and analysis.

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## Details

- Title: Initiation of Voluntary Recalls Under 21 CFR Part 7, Subpart C:  Guidance for Industry and FDA Staff
- Communication Type: Guidance Document
- Product Type: other
- Office Name: Office of Inspections and Investigations
- Office URL: /offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8
- Issue Date: 2022-03-04
- Last Changed: 2024-10-01
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2018-D-2074">FDA-2018-D-2074</a>

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