FDA Inspection 1205951 — Keurig/Dr. Pepper

Keurig/Dr. Pepper — FEI 3007466871

The FDA completed an inspection of Keurig/Dr. Pepper on Apr 25, 2023 in Tulsa, 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 25, 2023
Fiscal Year
2023
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Tulsa, OK (United States)

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