Regulations.gov document

Guidance for Industry on Requests for Feedback on Medical Device Submissions The…

Other · FDA-2012-D-0530 · posted Oct 3, 2017

Key facts

Document ID FDA-2012-D-0530-0031
Title Guidance for Industry on Requests for Feedback on Medical Device Submissions The Pre-Submission Program and Meetings with Food and Drug Administration Staff
Document type Other
Subtype Guidance
Agency FDA
Docket FDA-2012-D-0530
Posted Oct 3, 2017
Comment period opens Oct 3, 2017

At a glance

  • 10–99 Public comments on this docket

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