LifeSource-Upper Midwest OPO

Form 483

Minneapolis, Minnesota, United StatesFEI 3000718539Issued January 24, 2012

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3000718539.

Observations3

Issue DateJanuary 24, 2012

StatusNo Warning Letter

Related Inspections7

Establishment Details

Firm: LifeSource-Upper Midwest OPO
Location: Minneapolis, Minnesota, United States
FEI Number: 3000718539
Product Type: Biologics
Issue Date: January 24, 2012
Country: United States

Inspection History, 2010 to 2025

NAI6

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

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LifeSource-Upper Midwest OPO FDA Form 483, Minneapolis, Minnesota, January 24, 2012