FDA Inspection 976899 — 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 Jul 12, 2016 in Irving, TX. 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
Jul 12, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Irving, TX (United States)

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