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FDA Inspection 613139 — 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 September 17, 2009 in Irving, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 17, 2009
Fiscal Year
2009
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Irving, TX (United States)

Facility

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  • 815992 (VAI Thu Jan 31 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 771899 (OAI Tue Mar 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources