{"database": "openregs", "table": "documents", "rows": [["FDA-2014-D-1814-0050", "FDA", "FDA-2014-D-1814", "Reference 19 Experience of the Irish Blood Transfusion Service, Blood Products Advisory Committee re Bacterial Detection Testing by Blood Collection Establishments and Transfusion Services to Enhance the Safety and Availability of Platelets for Transfusion; Draft Guidance for Industry; Availability", "Supporting & Related Material", "Background Material", "2016-03-16T04:00:00Z", 2016, 3, null, null, "2016-03-16T16:39:01Z", null, 0, 0, "0900006481ec3c75"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2014-D-1814-0050"], "units": {}, "query_ms": 0.8183029713109136, "source": "Federal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"}