FDA Inspection 1181707 — Keurig Dr. Pepper Company

Keurig Dr. Pepper Company — FEI 1914562

The FDA completed an inspection of Keurig Dr. Pepper Company on Oct 6, 2022 in Saint Joseph, MO. 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 6, 2022
Fiscal Year
2023
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Saint Joseph, MO (United States)