FDA Inspection 805972 — Keurig Dr. Pepper
The FDA completed an inspection of Keurig Dr. Pepper on Oct 31, 2012 in Goodlettsville, TN. 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
- Oct 31, 2012
- Fiscal Year
- 2013
- Product Type
- Food/Cosmetics
- Project Area
- Food and Color Additives Petition Review
- Location
- Goodlettsville, TN (United States)