FDA Inspection 932712 — CoreRX Inc.

CoreRX Inc. — FEI 3007209985

The FDA completed an inspection of CoreRX Inc. on June 19, 2015 in Clearwater, FL. 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
June 19, 2015
Fiscal Year
2015
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Clearwater, FL (United States)