FDA Inspection 703042 — Nebraska Organ Recovery System d.b.a. Live On Nebraska

Nebraska Organ Recovery System d.b.a. Live On Nebraska — FEI 3003407913

The FDA completed an inspection of Nebraska Organ Recovery System d.b.a. Live On Nebraska on December 16, 2010 in Omaha, NE. 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 16, 2010
Fiscal Year
2011
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Omaha, NE (United States)

Citations

IDCFRDescription
1238121 CFR 1271.210(d)(2)Verification elements