FDA Inspection 638984 — Interfarma Corp.

Interfarma Corp. — FEI 3003605812

The FDA completed an inspection of Interfarma Corp. on Jan 20, 2010 in Miami, FL. 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
Jan 20, 2010
Fiscal Year
2010
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Miami, FL (United States)