{"database": "openregs", "table": "documents", "rows": [["FDA-2000-N-0038-0002", "FDA", "FDA-2000-N-0038", "Agency Information Collection Activities; Submission for OMB Review; Comment Request; Guidance for Industry: Submitting and Reviewing Complete Responses to Clinical Holds", "Notice", "General Notice", "2000-07-05T04:00:00Z", 2000, 7, "2000-07-05T04:00:00Z", "2000-08-05T03:59:59Z", "2025-06-04T23:30:59Z", "00-16813", 0, 0, "09000064804aeedb"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2000-N-0038-0002"], "units": {}, "query_ms": 0.3971270052716136, "source": "Federal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"}