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FDA Inspection 805924 — LifeSource-Upper Midwest OPO

LifeSource-Upper Midwest OPO — FEI 3000718539

The FDA completed an inspection of LifeSource-Upper Midwest OPO on October 24, 2012 in Minneapolis, MN. 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
October 24, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Minneapolis, MN (United States)

Facility

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  • 913084 (NAI Mon Feb 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 758993 (VAI Tue Jan 24 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources