FDA Inspection 929872 — Patheon UK Limited

Patheon UK Limited — FEI 3002807216

The FDA completed an inspection of Patheon UK Limited on May 8, 2015 in Swindon. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 8, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Swindon (United Kingdom)

Citations

IDCFRDescription
143421 CFR 211.42(c)(10)(iv)Environmental Monitoring System
145121 CFR 211.113(b)Procedures for sterile drug products
185221 CFR 211.94(a)Reactive/Additive/Absorptive Containers/Closures