{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where agency_id = \"FDA\", document_type = \"Other\" and posted_year = 2016 sorted by posted_date descending", "rows": [["FDA-2015-N-0101-1319", "FDA", "FDA-2015-N-0101", "Advice Letter from FDA CDER to American Chemistry Council", "Other", "Letter(s)", "2016-12-30T05:00:00Z", 2016, 12, "2016-12-30T05:00:00Z", null, "2016-12-30T18:11:04Z", null, 0, 0, "0900006482442595"], ["FDA-2015-D-0025-0016", "FDA", "FDA-2015-D-0025", "Medical Device Accessories \u2013 Describing Accessories and Classification Pathway for New Accessory Types Guidance for Industry and Food and Drug Administration Staff", "Other", "Guidance", "2016-12-30T05:00:00Z", 2016, 12, "2016-12-30T05:00:00Z", null, "2024-11-11T21:31:30Z", null, 1, 0, "09000064824410cc"], ["FDA-2016-D-0269-0113", "FDA", "FDA-2016-D-0269", "Prescription Requirement Under Section 503A of the Federal Food, Drug, and Cosmetic Act Guidance for Industry", 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