FDA Inspection 1141879 — Keurig Dr Pepper dba The American Bottling Company, Inc.

Keurig Dr Pepper dba The American Bottling Company, Inc. — FEI 2016934

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