FDA Inspection 1000697 — KEURIG DR PEPPER
The FDA completed an inspection of KEURIG DR PEPPER on Jan 12, 2017 in Cedar Rapids, 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
- Jan 12, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Cedar Rapids, IA (United States)