FDA Inspection 1098971 — EuroAPI Hungary Ltd.

EuroAPI Hungary Ltd. — FEI 3002806675

The FDA completed an inspection of EuroAPI Hungary Ltd. on Jun 21, 2019 in Budapest. 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
Jun 21, 2019
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Budapest (Hungary)

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