FDA Inspection 1268131 — Keurig Dr. Pepper

Keurig Dr. Pepper — FEI 2000047061

The FDA completed an inspection of Keurig Dr. Pepper on Apr 14, 2025 in Oklahoma City, OK. 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
Apr 14, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Oklahoma City, OK (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.