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FDA Inspection 919565 — PureTek Corporation

PureTek Corporation — FEI 1000125324

The FDA completed an inspection of PureTek Corporation on March 18, 2015 in San Fernando, CA. 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 18, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
San Fernando, CA (United States)

Facility

Other inspections at this facility

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  • 1116761 (VAI Thu Jan 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1034952 (VAI Fri Dec 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949735 (VAI Tue Oct 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 860979 (VAI Wed Dec 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources