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Guidance Documents/Guidance-Document/Notifying FDA of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section 506J of the FD&C Act: Guidance for Industry and Food and Drug Administration Staff

Notifying FDA of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section 506J of the FD&C Act: Guidance for Industry and Food and Drug Administration Staff

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

January 7, 2025

January 6, 2025

Center for Devices and Radiological Health

5d3b0ec7-bd9b-4b37-afcb-2bbba12501ad

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