FDA Inspection 768564 — Keurig Dr. Pepper
The FDA completed an inspection of Keurig Dr. Pepper on February 23, 2012 in Holland, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 23, 2012
- Fiscal Year
- 2012
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Holland, MI (United States)