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FDA Inspection 1028060 — 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 September 28, 2017 in Omaha, NE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 28, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Omaha, NE (United States)

Facility

Other inspections at this facility

  • 1227197 (NAI Fri Dec 29 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114057 (NAI Thu Nov 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 928793 (NAI Wed May 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817227 (NAI Tue Feb 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 703042 (VAI Thu Dec 16 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources