FDA Inspection 1210434 — Keurig Dr. Pepper

Keurig Dr. Pepper — FEI 3004274340

The FDA completed an inspection of Keurig Dr. Pepper on July 19, 2023 in Holland, MI. 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
July 19, 2023
Fiscal Year
2023
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Holland, MI (United States)