# LifeSource-Upper Midwest OPO - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1279132 - LifeSource-Upper Midwest OPO - 2025-07-30](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/e3c7c1bb-59d2-4df0-9dd5-ee3f8ac408a6) — source: FDA, date: July 30, 2025
- [FDA Inspection 1279132 - LifeSource-Upper Midwest OPO - 2025-07-30](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/d789f524-d6b3-49fb-aac8-fdad12a32839) — classification: No Action Indicated (NAI), source: FDA, date: July 30, 2025
- [FDA Inspection 1084827 - LifeSource-Upper Midwest OPO - 2019-03-22](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/2eaa755d-6818-4d92-ab44-0ca5694638a5) — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2019
- [FDA Inspection 1084827 - LifeSource-Upper Midwest OPO - 2019-03-22](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/ea2a40de-1ad7-4654-9f61-a83cbb3ae9df) — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2019
- [FDA Inspection 1028803 - LifeSource-Upper Midwest OPO - 2017-09-20](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/4c7221c7-c03a-4f24-9ce6-06f138b91e74) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- [FDA Inspection 1028803 - LifeSource-Upper Midwest OPO - 2017-09-20](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/7bc134d2-aaec-46de-84dd-d4e2560fefd5) — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2017
- [FDA Inspection 913084 - LifeSource-Upper Midwest OPO - 2015-02-09](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/79c37416-78e0-465f-92b5-3415eac97095) — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2015
- [FDA Inspection 805924 - LifeSource-Upper Midwest OPO - 2012-10-24](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/bdfc812a-123f-476e-b936-f05fabf7ce32) — 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](https://www.keypedia.com/records/fda_inspections/lifesource-upper-midwest-opo/0cdee184-7db6-471c-9b1b-9bf33cb6ab8d) — classification: No Action Indicated (NAI), source: FDA, date: May 21, 2010

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