FDA Inspection 1059778 — AAK USA K1-K2 LLC

AAK USA K1-K2 LLC — FEI 1037097

The FDA completed an inspection of AAK USA K1-K2 LLC on June 18, 2018 in Louisville, KY. 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 18, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Louisville, KY (United States)