FDA Inspection 1098252 — Patheon UK Limited

Patheon UK Limited — FEI 3002807216

The FDA completed an inspection of Patheon UK Limited on March 1, 2018 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
March 1, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Swindon (United Kingdom)

Additional Details

Mutual Recognition Agreement (MRA)