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 Sep 17, 2009 in Irving, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Food/Cosmetics.