FDA Inspection 756729 — American Needle

American Needle — FEI 3004696168

The FDA completed an inspection of American Needle on December 5, 2011 in Buffalo Grove, 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
December 5, 2011
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Buffalo Grove, IL (United States)