FDA Inspection 1329638 — Fermion Oy

Fermion Oy — FEI 3003491490

The FDA completed an inspection of Fermion Oy on Feb 25, 2026 in Espoo. 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
Feb 25, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Espoo (Finland)

Additional Details

Mutual Recognition Agreement (MRA)