FDA Inspection 1309538 — Orion Corporation, Orion Pharma

Orion Corporation, Orion Pharma — FEI 3003743938

The FDA completed an inspection of Orion Corporation, Orion Pharma on April 25, 2024 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
April 25, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Turku (Finland)

Additional Details

Mutual Recognition Agreement (MRA)