FDA Inspection 680645 — Orion Corporation, Orion Pharma

Orion Corporation, Orion Pharma — FEI 3003743938

The FDA completed an inspection of Orion Corporation, Orion Pharma on September 3, 2010 in Turku. 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
September 3, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Turku (Finland)