{"database": "openregs", "table": "documents", "rows": [["FDA-2008-D-0233-0003", "FDA", "FDA-2008-D-0233", "Draft Guidance for Industry: Use of Nucleic Acid Tests to Reduce the Risk of Transmission of West Nile Virus From Donors of Whole Blood and Blood Components Intended for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 Cells, Tissues, and Cellular and Tissue-Based Products; Request for Data", "Notice", "NRD-Notice of Requesting Data, Info, & Views", "2008-07-07T04:00:00Z", 2008, 7, "2008-07-07T04:00:00Z", null, "2008-07-07T11:57:02Z", "E8-15368", 0, 0, "090000648065a4ee"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2008-D-0233-0003"], "units": {}, "query_ms": 0.8776800241321325, "source": "Federal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"}