FDA Inspection 843279 — Keurig Dr Pepper
The FDA completed an inspection of Keurig Dr Pepper on Aug 6, 2013 in Reno, NV. 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
- Aug 6, 2013
- Fiscal Year
- 2013
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Reno, NV (United States)