documents: FDA-2005-D-0140-0009
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0140-0009 | FDA | FDA-2005-D-0140 | Reference 9 - Federal Register, August 24, 2007 (72 FR 48765), Current Good Manufacturing Practice for Blood and Blood Components; Notification of Consignees and Transfussion Recipients Receiving Blood and Blood Components at Increased Risk of Transmitting Hepatitis C Virus Infection ("Lookback"); Final Rule | Supporting & Related Material | BKG-Background Material | 2010-04-30T04:00:00Z | 2010 | 4 | 2010-04-30T15:18:15Z | 0 | 0 | 0900006480ae387b |
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- 0 rows from regs_document_id in fr_regs_crossref