FDA Inspection 909185 — Keurig/Dr. Pepper
The FDA completed an inspection of Keurig/Dr. Pepper on Dec 10, 2014 in Tulsa, 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
- Dec 10, 2014
- Fiscal Year
- 2015
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Tulsa, OK (United States)