FDA Inspection 658178 — Lafeber Company

Lafeber Company — FEI 1484030

The FDA completed an inspection of Lafeber Company on Apr 21, 2010 in Cornell, IL. 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
Apr 21, 2010
Fiscal Year
2010
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Cornell, IL (United States)