FDA Inspection 944830 — Biovian Oy

Biovian Oy — FEI 3004523978

The FDA completed an inspection of Biovian Oy on September 25, 2015 in Turku. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 25, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Turku (Finland)