FDA Inspection 655748 — Keurig Dr. Pepper
The FDA completed an inspection of Keurig Dr. Pepper on April 5, 2010 in Goodlettsville, TN. 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
- April 5, 2010
- Fiscal Year
- 2010
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Goodlettsville, TN (United States)