FDA Inspection 846992 — EMF Limited

EMF Limited — FEI 3001558627

The FDA completed an inspection of EMF Limited on August 15, 2013 in Winnipeg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 15, 2013
Fiscal Year
2013
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Winnipeg (Canada)