FDA Inspection 1092893 — Keurig Dr Pepper

Keurig Dr Pepper — FEI 2924979

The FDA completed an inspection of Keurig Dr Pepper on June 5, 2019 in Sacramento, CA. 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
June 5, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Sacramento, CA (United States)