FDA Inspection 781927 — Intervet Inc

Intervet Inc — FEI 1924403

The FDA completed an inspection of Intervet Inc on May 17, 2012 in Omaha, NE. 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
May 17, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Omaha, NE (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.