FDA Inspection 911478 — CherryFlex Inc.

CherryFlex Inc. — FEI 3004751837

The FDA completed an inspection of CherryFlex Inc. on January 23, 2015 in Traverse City, MI. 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
January 23, 2015
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Traverse City, MI (United States)