documents: FDA-2001-N-0105-0002
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| posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |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-2001-N-0105-0002 | FDA | FDA-2001-N-0105 | Agency Information Collection Activities; Submission for OMB Review; Comment Request; Medical Devices; Third-Party Premarket Submission Review and Quality System Inspections Under United States/European Community Mutual Recognition Agreement | Notice | 30 Day Proposed Information Collection | 2002-01-14T05:00:00Z | 2002 | 1 | 2002-01-14T05:00:00Z | 2002-02-14T04:59:59Z | 2025-02-03T14:55:57Z | 02-854 | 0 | 0 | 09000064804bafe5 |
Links from other tables
- 1 row from regs_document_id in fr_regs_crossref