FDA Inspection 1310408 — Orion Corporation, Orion Pharma

Orion Corporation, Orion Pharma — FEI 3003073605

The FDA completed an inspection of Orion Corporation, Orion Pharma on November 7, 2024 in Espoo. 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
November 7, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Espoo (Finland)

Additional Details

Mutual Recognition Agreement (MRA)