FDA Inspection 1304156 — Isteka

Isteka — FEI 1000581735

The FDA completed an inspection of Isteka on January 29, 2026 in Reykjavik. 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
January 29, 2026
Fiscal Year
2026
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Reykjavik (Iceland)