FDA Inspection 1282064 — The American Bottling Company DBA Keurig Dr. Pepper
The FDA completed an inspection of The American Bottling Company DBA Keurig Dr. Pepper on September 5, 2025 in Indianapolis, IN. 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
- September 5, 2025
- Fiscal Year
- 2025
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Indianapolis, IN (United States)