FDA Inspection 939702 — Keurig Dr. Pepper, Inc.
The FDA completed an inspection of Keurig Dr. Pepper, Inc. on Sep 2, 2015 in Carteret, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 2, 2015
- Fiscal Year
- 2015
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Carteret, NJ (United States)