FDA Inspection 1310192 — Keurig Dr. Pepper

Keurig Dr. Pepper — FEI 2000047510

The FDA completed an inspection of Keurig Dr. Pepper on February 26, 2026 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
February 26, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Goodlettsville, TN (United States)