FDA Inspection 594562 — Patheon UK Limited

Patheon UK Limited — FEI 3002807216

The FDA completed an inspection of Patheon UK Limited on June 24, 2009 in Swindon. 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 24, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Swindon (United Kingdom)