FDA Inspection 818915 — Midwest Syrup Company

Midwest Syrup Company — FEI 1920348

The FDA completed an inspection of Midwest Syrup Company on Feb 13, 2013 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
Feb 13, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Kansas City, MO (United States)