FDA Inspection 1065473 — Keurig Dr. Pepper, Inc.
The FDA completed an inspection of Keurig Dr. Pepper, Inc. on Sep 12, 2018 in Carteret, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 12, 2018
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Carteret, NJ (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 12753 | 21 CFR 120.11(a)(1)(iv)(B) | CA record review adequacy |
| 9954 | 21 CFR 120.11(a)(1)(iv) | Verification - CCP, CA record review |