FDA Inspection 1029746 — Epax Norway AS

Epax Norway AS — FEI 2000008099

The FDA completed an inspection of Epax Norway AS on September 22, 2017 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
September 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Alesund (Norway)