documents: FDA-2022-N-0150-0011
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2022-N-0150-0011 | FDA | FDA-2022-N-0150 | Revocation of Authorization of Emergency Use of In Vitro Diagnostic Device for Detection and/or Diagnosis of COVID–19; Availability | Notice | Announcement | 2024-07-25T04:00:00Z | 2024 | 7 | 2024-07-25T04:00:00Z | 2024-08-13T13:56:38Z | 2024-16345 | 0 | 0 | 09000064866050dc |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref