FDA Inspection 862165 — Keurig Dr. Pepper
The FDA completed an inspection of Keurig Dr. Pepper on Jan 15, 2014 in Holland, MI. 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 15, 2014
- Fiscal Year
- 2014
- Product Type
- Food/Cosmetics
- Project Area
- Food and Color Additives Petition Review
- Location
- Holland, MI (United States)