documents: FDA-2008-D-0031-0001
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2008-D-0031-0001 | FDA | FDA-2008-D-0031 | Guidance for Industry and Food and Drug Administration Staff; Clinical Laboratory Improvement Amendments of 1988: Recommendations for Clinical Laboratory Improvement Amendments of 1988: Waiver Applications for Manufacturers of In Vitro Diagnostic Devices; Availability | Notice | NAD-Notice of Availability of Data | 2008-01-30T05:00:00Z | 2008 | 1 | 2008-01-30T05:00:00Z | 2009-01-31T04:59:59Z | 2024-11-12T04:09:45Z | E8-01557 | 1 | 0 | 09000064803a4a6b |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref