FDA Inspection 733195 — Upjohn Manufacturing Ireland Unlimited Company

Upjohn Manufacturing Ireland Unlimited Company — FEI 3003382089

The FDA completed an inspection of Upjohn Manufacturing Ireland Unlimited Company on June 17, 2011 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
June 17, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cork (Ireland)