FDA Inspection 1027446 — CoreFX Ingredients LLC

CoreFX Ingredients LLC — FEI 1420872

The FDA completed an inspection of CoreFX Ingredients LLC on September 20, 2017 in Orangeville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 20, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Orangeville, IL (United States)