documents: FDA-2005-N-0161-0006
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-0161-0006 | FDA | FDA-2005-N-0161 | Agency Information Collection Activities; Proposed Collection; Comment Request; Current Good Manufacturing Practices and Related Regulations for Blood and Blood Components; and Requirements for Donor Testing, Donor Notification, and ‘‘Lookback’’ | Notice | 60 Day Proposed Information Collection | 2014-10-20T04:00:00Z | 2014 | 10 | 2014-10-20T04:00:00Z | 2014-12-20T04:59:59Z | 2025-07-02T17:18:24Z | 2014-24797 | 0 | 0 | 09000064818dcd67 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref