FDA Inspection 572921 — CherryFlex Inc.

CherryFlex Inc. — FEI 3004751837

The FDA completed an inspection of CherryFlex Inc. on March 24, 2009 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
March 24, 2009
Fiscal Year
2009
Product Type
Food/Cosmetics
Project Area
Food and Color Additives Petition Review
Location
Traverse City, MI (United States)