FDA Inspection 1066899 — Fermion Oy

Fermion Oy — FEI 3002807817

The FDA completed an inspection of Fermion Oy on September 14, 2018 in Hanko Pohjoinen. 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 14, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hanko Pohjoinen (Finland)