FDA Inspection 1141879 — Keurig Dr Pepper

Keurig Dr Pepper — FEI 2016934

The FDA completed an inspection of Keurig Dr Pepper on Mar 17, 2021 in Vernon, CA. 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
Mar 17, 2021
Fiscal Year
2021
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Vernon, CA (United States)

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