FDA Inspection 804261 — Keurig Dr Pepper Inc.

Keurig Dr Pepper Inc. — FEI 1622841

The FDA completed an inspection of Keurig Dr Pepper Inc. on Oct 22, 2012 in Austin, 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
Oct 22, 2012
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Austin, TX (United States)

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