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 Aug 28, 2013 in Louisville, KY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.