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FDA Inspection 616347 — Advanced Sterilization Products

Advanced Sterilization Products — FEI 3003662624

The FDA completed an inspection of Advanced Sterilization Products on September 28, 2009 in Irvine, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 28, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

Facility

Other inspections at this facility

  • 948179 (NAI Wed Oct 28 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 853825 (VAI Fri Nov 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 788386 (OAI Thu Jun 21 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 702976 (VAI Fri Dec 17 2010 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 669654 (NAI Wed Jun 16 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources