{"database": "openregs", "table": "documents", "rows": [["FDA-2009-D-0137-0039", "FDA", "FDA-2009-D-0137", "Reference 10  FDA Blood Products Advisory Committee T. cruzi Incidence Study in Blood Donors and its Implications for One-time Testing of Blood Donors August 2 2011", "Supporting & Related Material", "Background Material", "2016-11-10T05:00:00Z", 2016, 11, null, null, "2016-11-10T15:31:20Z", null, 0, 0, "09000064823877ef"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2009-D-0137-0039"], "units": {}, "query_ms": 74.7036850079894, "source": "Federal Register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"}