{"database": "openregs", "table": "documents", "rows": [["FDA-2003-N-0251-0001", "FDA", "FDA-2003-N-0251", "Agency Emergency Processing Under OMB Review; Inspection by Accredited Persons Program Under the Medical Device User Fee and Modernization Act of 2002", "Notice", "General Notice", "2003-05-01T04:00:00Z", 2003, 5, "2003-04-28T04:00:00Z", "2003-05-29T03:59:59Z", "2025-02-25T12:27:20Z", "03-10414", 0, 0, "090000648048f5ef"]], "columns": ["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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2003-N-0251-0001"], "units": {}, "query_ms": 25.474721915088594, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}