# Guidance on Section 216 of the Food and Drug Administration Modernization Act of 1997 - Guidance for Industry and for FDA Reviewers - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/guidance-on-section-216-of-the-food-and-drug-administration-modernization-act-of-1997-guidance-for-industry-and-for-fda-reviewers/0e9d60c0-b3c7-4651-a785-9107ddbc73e6

> FDA guidance document: Guidance on Section 216 of the Food and Drug Administration Modernization Act of 1997 - Guidance for Industry and for FDA Reviewers. Issue date: August 08, 2000. Get complete insights and analysis.

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## Details

- Title: Guidance on Section 216 of the Food and Drug Administration Modernization Act of 1997 - Guidance for Industry and for FDA Reviewers
- 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: 2000-08-08
- Last Changed: 2020-03-18
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2020-D-0957">FDA-2020-D-0957</a>

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