{"providers":[{"id":"ddapi_inspections","label":"FDA inspection classifications (OAI/VAI/NAI)","enabled":true,"host":"https://api-datadashboard.fda.gov/v1","access":"keyed-but-free DDAPI POST (Authorization-User + Authorization-Key)","license":"US-gov public domain"},{"id":"ddapi_compliance","label":"FDA compliance actions (warning letters / injunctions / seizures)","enabled":true,"host":"https://api-datadashboard.fda.gov/v1","access":"keyed-but-free DDAPI POST","license":"US-gov public domain"},{"id":"ddapi_citations","label":"FDA Form-483 inspection citations","enabled":true,"host":"https://api-datadashboard.fda.gov/v1","access":"keyed-but-free DDAPI POST","license":"US-gov public domain"},{"id":"ddapi_import_refusals","label":"FDA import refusals (OASIS)","enabled":true,"host":"https://api-datadashboard.fda.gov/v1","access":"keyed-but-free DDAPI POST","license":"US-gov public domain"},{"id":"openfda_recalls","label":"openFDA enforcement/recall reports (cross-ref)","enabled":false,"host":null,"access":"keyless openFDA — DEFERRED (overlaps the recall sibling; cross-ref only)","license":"US-gov public domain"},{"id":"warning_letters_fulltext","label":"FDA Warning Letters full-text corpus","enabled":false,"host":null,"access":"keyless HTML (fda.gov) — DEFERRED, a future sub-idea flips this row","license":"US-gov public domain"}],"primary_host":"https://api-datadashboard.fda.gov/v1","key_configured":true,"coverage":{"included":["ddapi_inspections","ddapi_compliance","ddapi_citations","ddapi_import_refusals"],"deferred":["openfda_recalls","warning_letters_fulltext"],"product_types":["Drugs","Devices","Biologics","Foods","Cosmetics","Tobacco","Veterinary","Radiological Health"],"foreign_facilities":true},"scoring_dimensions":["oai_classification","critical_action","warning_letter","citations_483","import_refusals","recency","trend","history"],"rating_bands":[{"min_score":75,"rating":"critical"},{"min_score":50,"rating":"high"},{"min_score":20,"rating":"medium"},{"min_score":0,"rating":"low"}],"freshness_note":"An FDA inspection classification (OAI/VAI/NAI) is posted only AFTER the inspection closes, so open/recent cases may lack a classification or 483 citation data. FEI numbers are global, so foreign manufacturers (India/China/ EU) are covered (see CountryName). Live per-call DDAPI queries only (no bulk redistribution).","key_note":"The FDA Data Dashboard API is keyed-but-FREE: a one-time email-issued Authorization-Key (https://datadashboard.fda.gov/oii/api/index.htm). The key is runtime config; absent => the paid /fda/* grains return available:false and this service stays up.","note":"Provenance, licensing and coverage of the public FDA establishment-enforcement records the paid /fda/* routes fuse over. US-gov public domain; the value-add is the FEI resolve + four-stream fusion + deterministic risk score, not a resale. openFDA recalls + the warning-letters full-text corpus are registered as deferred datasets a future sub-idea enables.","attribution":["FDA Data Dashboard REST API (US Food & Drug Administration, api-datadashboard.fda.gov; US-gov public domain): inspections_classifications, compliance_actions, inspections_citations, import_refusals."],"disclaimer":"These are automated GMP / regulatory-compliance RISK INDICATORS derived from public FDA establishment-enforcement records, NOT legal, regulatory, medical or investment advice and NOT a guarantee. They describe a MANUFACTURER's regulatory standing, not the safety of any specific product. FDA data lags: an inspection classification is posted only after the inspection closes, and open cases may lack citation data. Verify inspection status, warning-letter close-out and current enforcement directly with FDA before relying on them."}