FDA Inspection 996665 — Bunzl Kansas City

Bunzl Kansas City — FEI 3004688750

The FDA completed an inspection of Bunzl Kansas City on Nov 4, 2016 in Kansas City, 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 4, 2016
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Kansas City, MO (United States)