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
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Clearwater, FL (United States)