documents: FDA-2012-D-0530-0031

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2012-D-0530-0031 FDA FDA-2012-D-0530 Guidance for Industry on Requests for Feedback on Medical Device Submissions The Pre-Submission Program and Meetings with Food and Drug Administration Staff Other Guidance 2017-10-03T04:00:00Z 2017 10 2017-10-03T04:00:00Z   2024-11-07T01:17:02Z   1 0 0900006482b95aad

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