FDA Inspection 733396 — Isteka

Isteka — FEI 1000581735

The FDA completed an inspection of Isteka on June 23, 2011 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 23, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Reykjavik (Iceland)