# Medtronic Perfusion Systems, Brooklyn Park, MN – FDA Inspections

Source: https://www.keypedia.com/companies/medtronic-perfusion-systems/213f3751-a903-4fee-af09-e7e6ee04e728

> Inspection records and compliance data for Medtronic Perfusion Systems in Brooklyn Park, Minnesota. 8 FDA inspections on record, last inspected June 23, 2022.

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## Details

- Name: Medtronic Perfusion Systems
- FEI Number: 1000116158
- Address Line 1: 7611 Northland Dr N
- City: Brooklyn Park
- State: Minnesota
- Zip Code: 55428
- Country Name: United States
- Address: 7611 Northland Dr N, Brooklyn Park, Minnesota 55428, United States
- Country: United States

## Related Documents

- FDA Inspection 1178299 - Medtronic Perfusion Systems - 2022-06-23 — classification: No Action Indicated (NAI), source: FDA, date: June 23, 2022
- [FDA Inspection 987452 - Medtronic Perfusion Systems - 2016-09-30](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/824b6add-4362-4992-9175-dec9fc4a088f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2016
- FDA Inspection 987452 - Medtronic Perfusion Systems - 2016-09-30 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2016
- FDA Inspection 886720 - Medtronic Perfusion Systems - 2014-06-24 — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2014
- FDA Inspection 867900 - Medtronic Perfusion Systems - 2014-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2014
- FDA Inspection 831904 - Medtronic Perfusion Systems - 2013-04-01 — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2013
- FDA Inspection 831904 - Medtronic Perfusion Systems - 2013-04-01 — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2013
- FDA Inspection 764709 - Medtronic Perfusion Systems - 2012-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2012
- FDA Inspection 764709 - Medtronic Perfusion Systems - 2012-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2012
- FDA Inspection 667045 - Medtronic Perfusion Systems - 2010-06-15 — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2010

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