FDA Inspection 975285 — Fermion OY

Fermion OY — FEI 3003340711

The FDA completed an inspection of Fermion OY on June 3, 2016 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
June 3, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oulu (Finland)