FDA Inspection 1017156 — CherryFlex Inc.

CherryFlex Inc. — FEI 3004751837

The FDA completed an inspection of CherryFlex Inc. on June 29, 2017 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
June 29, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Traverse City, MI (United States)