{"database": "openregs", "table": "documents", "rows": [["FDA-2015-D-1211-0020", "FDA", "FDA-2015-D-1211", "Ref. 17 FDA Blood Products Advisory Committee Meeting, December 11-12, 1997 re Revised Recommendations for Reducing the Risk of Human Immunodeficiency Virus Transmission by Blood and Blood Products; Draft Guidance for Industry", "Supporting & Related Material", "Background Material", "2015-05-18T04:00:00Z", 2015, 5, null, null, "2015-05-18T18:45:00Z", null, 0, 0, "0900006481ae6a9c"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2015-D-1211-0020"], "units": {}, "query_ms": 98.32721599377692, "source": "Federal Register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"}