documents: FDA-2017-D-6530-0001

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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2017-D-6530-0001 FDA FDA-2017-D-6530 Formal Meetings Between the Food and Drug Administration and Sponsors or Applicants of Prescription Drug User Fee Act Products; Draft Guidance for Industry; Availability Notice Notice of Availability 2017-12-29T05:00:00Z 2017 12 2017-12-29T05:00:00Z 2018-03-30T03:59:59Z 2018-03-28T01:02:41Z 2017-28140 0 0 0900006482d832bd

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