{"database": "openregs", "table": "documents", "rows": [["FDA-2010-P-0176-0025", "FDA", "FDA-2010-P-0176", "FDA/CDRH Ombudsman Response to Ethicon Endo-Surgery, Inc., November 18, 2010 - Letter", "Other", "LET-Letter", "2011-05-24T04:00:00Z", 2011, 5, "2011-05-24T04:00:00Z", null, "2013-08-11T01:41:47Z", null, 0, 0, "0900006480ddf990"]], "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"posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2010-P-0176-0025"], "units": {}, "query_ms": 0.3224849933758378, "source": "Federal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"}