FDA Inspection 1048122 — Keurig Dr. Pepper
The FDA completed an inspection of Keurig Dr. Pepper on Mar 7, 2018 in Oklahoma City, OK. 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
- Mar 7, 2018
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Oklahoma City, OK (United States)