FDA Inspection 1092893 — Keurig Dr Pepper
The FDA completed an inspection of Keurig Dr Pepper on Jun 5, 2019 in Sacramento, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 5, 2019
- Fiscal Year
- 2019
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Sacramento, CA (United States)