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FDA Inspection 968506 — PQ Corporation

PQ Corporation — FEI 1421453

The FDA completed an inspection of PQ Corporation on April 18, 2016 in Utica, IL. 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
April 18, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Utica, IL (United States)

Facility

Other inspections at this facility

  • 1166227 (VAI Tue Feb 22 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1086561 (VAI Tue Apr 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1013994 (VAI Wed May 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859640 (VAI Thu Dec 19 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 737674 (VAI Tue Aug 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources