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FDA of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section 506J of the FD&C Act; Draft Guidance for Industry and Food and Drug Administration Staff; Availability

2 organizations filed 3 public comments on Notifying FDA of a Permanent Discontinuance or Interruption in Manufacturing of a Device Under Section 506J of the FD&C Act; Draft Guidance for Industry and Food and Drug Administration Staff; Availability, at the Food and Drug Administration. The comment window closed 894d ago.

Commenters (2)

• Advanced Medical Technology Associationtrade assoc.

  2 filings · confidence 97%
• Medical Imaging & Technology Alliancetrade assoc.

  1 filing · confidence 97%