documents: FDA-2005-D-0140-0019

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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posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id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-2005-D-0140-0019 FDA FDA-2005-D-0140 Reference 8 Federal Register, December 14, 1999 (64 FR 71147), Guidance for Industry: In the Manufacture and Clinical Evaluation of In Vitro Tests to Detect Nucleic Acid Sequences of Human Immunodeficiency Viruses Types 1 and 2, December 1999. Supporting & Related Material Background Material 2017-12-28T05:00:00Z 2017 12     2017-12-28T20:40:08Z   0 0 0900006482d7ee4f

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