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

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

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

August 8, 2000

March 18, 2020

Center for Devices and Radiological Health

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