FDA Inspection 1048122 — Keurig Dr. Pepper
The FDA completed an inspection of Keurig Dr. Pepper on March 7, 2018 in Oklahoma City, OK. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- March 7, 2018
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Oklahoma City, OK (United States)