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FDA Inspection 752701 — Organ Recovery Systems, Inc.

Organ Recovery Systems, Inc. — FEI 3004068499

The FDA completed an inspection of Organ Recovery Systems, Inc. on November 8, 2011 in Itasca, IL. 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
November 8, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Itasca, IL (United States)

Facility

Other inspections at this facility

  • 1071339 (NAI Tue Oct 16 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1001720 (OAI Fri Feb 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 921541 (NAI Tue Apr 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 634996 (VAI Wed Dec 09 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources