FDA Inspection 1076128 — Keurig Dr Pepper
The FDA completed an inspection of Keurig Dr Pepper on Nov 6, 2018 in Des Moines, IA. 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
- Nov 6, 2018
- Fiscal Year
- 2019
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Des Moines, IA (United States)