documents: FDA-2005-D-0140-0014
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| 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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0140-0014 | FDA | FDA-2005-D-0140 | Reference 3 FDA Memorandum to All Registered Blood Establishments: “Revised Recommendations for Testing Whole Blood, Blood Components, Source Plasma and Source Leukocytes for Antibody to Hepatitis C Virus Encoded Antigen (Anti-HCV),” August 5, 1993. | Supporting & Related Material | Background Material | 2017-12-28T05:00:00Z | 2017 | 12 | 2017-12-28T20:40:33Z | 0 | 0 | 0900006482d7ee41 |
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- 0 rows from regs_document_id in fr_regs_crossref