{"database": "openregs", "table": "documents", "rows": [["FDA-2008-D-0233-0001", "FDA", "FDA-2008-D-0233", "Draft Guidance for Industry: Use of Nucleic Acid Tests to Reduce the Risk of Transmission of West Nile Virus from Donors of Whole Blood and Blood Components Intended for Transfusion and Donors of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps); Availability", "Notice", "NAD-Notice of Availability of Data", "2008-04-28T04:00:00Z", 2008, 4, "2008-04-28T04:00:00Z", "2008-07-29T03:59:59Z", "2024-11-12T04:13:44Z", "E8-09253", 1, 0, "0900006480537ea6"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2008-D-0233-0001"], "units": {}, "query_ms": 29.269283986650407, "source": "Federal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"}