FDA Inspection 1066899 — Fermion Oy

Fermion Oy — FEI 3002807817

The FDA completed an inspection of Fermion Oy on Sep 14, 2018 in Hanko Pohjoinen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 14, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hanko Pohjoinen (Finland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.