# LifeSource-Upper Midwest OPO, Minneapolis, MN – FDA Inspections

Source: https://www.keypedia.com/companies/lifesource-upper-midwest-opo/30344509-970e-4f39-9a9c-dcd0da459653

> Inspection records and compliance data for LifeSource-Upper Midwest OPO in Minneapolis, Minnesota. 7 FDA inspections on record, last inspected July 30, 2025.

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## Details

- Name: LifeSource-Upper Midwest OPO
- FEI Number: 3000718539
- Address Line 1: 2225 W River Rd
- City: Minneapolis
- State: Minnesota
- Zip Code: 55411
- Country Name: United States
- Address: 2225 W River Rd, Minneapolis, Minnesota 55411, United States
- Country: United States

## Related Documents

- FDA Inspection 1279132 - LifeSource-Upper Midwest OPO - 2025-07-30 — source: FDA, date: July 30, 2025
- FDA Inspection 1279132 - LifeSource-Upper Midwest OPO - 2025-07-30 — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2025
- FDA Inspection 1084827 - LifeSource-Upper Midwest OPO - 2019-03-22 — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2019
- FDA Inspection 1084827 - LifeSource-Upper Midwest OPO - 2019-03-22 — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2019
- FDA Inspection 1028803 - LifeSource-Upper Midwest OPO - 2017-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- FDA Inspection 1028803 - LifeSource-Upper Midwest OPO - 2017-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- FDA Inspection 913084 - LifeSource-Upper Midwest OPO - 2015-02-09 — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2015
- FDA Inspection 805924 - LifeSource-Upper Midwest OPO - 2012-10-24 — classification: No Action Indicated (NAI), source: FDA, date: October 24, 2012
- [FDA Inspection 758993 - LifeSource-Upper Midwest OPO - 2012-01-24](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/4b6a0a3e-0caa-4355-a42b-2dcfa7e8c5a7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 24, 2012
- FDA Inspection 666938 - LifeSource-Upper Midwest OPO - 2010-05-21 — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2010

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