documents: FDA-2005-N-0161-0007
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-N-0161-0007 | FDA | FDA-2005-N-0161 | Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Current Good Manufacturing Practices and Related Regulations for Blood and Blood Components; and Requirements for Donor Testing, Donor Notification, and ‘‘Lookback’’ | Notice | 30 Day Proposed Information Collection | 2015-03-03T05:00:00Z | 2015 | 3 | 2015-03-03T05:00:00Z | 2015-04-03T03:59:59Z | 2025-07-02T17:20:41Z | 2015-04381 | 0 | 0 | 0900006481a26cb7 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref