FDA Inspection 1223510 — Fermion Oy

Fermion Oy — FEI 3003491490

The FDA completed an inspection of Fermion Oy on November 24, 2023 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
November 24, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Espoo (Finland)