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documents: FDA-2025-D-1504-0002

Federal regulatory documents currently open for public comment.

Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2025-D-1504-0002 FDA FDA-2025-D-1504 Responding to FDA Form 483 Observations at the Conclusion of a Drug CGMP Inspection: Draft Guidance for Industry Other Guidance 2026-03-09 2026 3 2026-03-09 2026-05-09 2026-04-10 09:00:26   1 0 09000064b9200f6d
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