FDA Inspection 1316126 — Upjohn Manufacturing Ireland Unlimited Company

Upjohn Manufacturing Ireland Unlimited Company — FEI 3003382089

The FDA completed an inspection of Upjohn Manufacturing Ireland Unlimited Company on January 26, 2024 in Cork. 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
January 26, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cork (Ireland)

Additional Details

Mutual Recognition Agreement (MRA)