FDA Inspection 634996 — Organ Recovery Systems, Inc.

Organ Recovery Systems, Inc. — FEI 3004068499

The FDA completed an inspection of Organ Recovery Systems, Inc. on December 9, 2009 in Itasca, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 9, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Itasca, IL (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures