FDA Inspection 749408 — American Bottling Co. - Keurig Dr Pepper

American Bottling Co. - Keurig Dr Pepper — FEI 1624836

The FDA completed an inspection of American Bottling Co. - Keurig Dr Pepper on October 4, 2011 in Irving, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 4, 2011
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Irving, TX (United States)

Citations

IDCFRDescription
156021 CFR 110.35(c)Lack of effective pest exclusion