FDA Inspection 1084402 — Dr Pepper/Seven Up Manufacturing Company

Dr Pepper/Seven Up Manufacturing Company — FEI 3002914068

The FDA completed an inspection of Dr Pepper/Seven Up Manufacturing Company on Nov 27, 2018 in Saint Louis, MO. 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
Nov 27, 2018
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Saint Louis, MO (United States)