FDA Inspection 854875 — Epax Norway AS

Epax Norway AS — FEI 2000008099

The FDA completed an inspection of Epax Norway AS on October 10, 2013 in Alesund. 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
October 10, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Alesund (Norway)