FDA Inspection 1022585 — PQ Silica UK Ltd

PQ Silica UK Ltd — FEI 3003924590

The FDA completed an inspection of PQ Silica UK Ltd on July 21, 2017 in Warrington. 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
July 21, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Warrington (United Kingdom)