FDA Inspection 845978 — AAK USA K1-K2 LLC

AAK USA K1-K2 LLC — FEI 1037097

The FDA completed an inspection of AAK USA K1-K2 LLC on August 28, 2013 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 28, 2013
Fiscal Year
2013
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Louisville, KY (United States)