dockets: FDA-2005-N-0161
This data as json
| id | agency_id | title | docket_type | last_modified | object_id |
|---|---|---|---|---|---|
| FDA-2005-N-0161 | FDA | Current Good Manufacturing Practices and Related Regulations for Blood and Blood Components; and Requirements for Donor Testing, Donor Notification, and Lookback | Nonrulemaking | 2022-01-05T01:02:15Z | 0b000064804403d1 |
Links from other tables
- 8 rows from docket_id in documents