FDA Inspection 1124625 — Fermion OY

Fermion OY — FEI 3003340711

The FDA completed an inspection of Fermion OY on February 12, 2020 in Oulu. 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
February 12, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oulu (Finland)

Additional Details

Mutual Recognition Agreement (MRA)