documents: FDA-2011-D-0799-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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| FDA-2011-D-0799-0001 | FDA | FDA-2011-D-0799 | Draft Guidance for Industry: Use of Nucleic Acid Tests on Pooled and Individual Samples From Donors of Whole Blood and Blood Components, Including Source Plasma, to Reduce the Risk of Transmission of Hepatitis B Virus | Notice | Notice of Availability | 2011-11-28T05:00:00Z | 2011 | 11 | 2011-11-28T05:00:00Z | 2012-01-28T04:59:59Z | 2015-04-03T22:40:47Z | 2011-30449 | 0 | 0 | 0900006480f74467 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref