# Medtronic Perfusion Systems - Inspection Records

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. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1178299 - Medtronic Perfusion Systems - 2022-06-23](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/2e9808ed-2d24-4c75-a798-711ec2fd971d) — 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](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/66cb9e0a-1b6a-4615-b785-1b69b9d49405) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 30, 2016
- [FDA Inspection 886720 - Medtronic Perfusion Systems - 2014-06-24](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/c369a168-85f1-46d7-bd0e-9efe4a79bdd6) — classification: No Action Indicated (NAI), source: FDA, date: June 24, 2014
- [FDA Inspection 867900 - Medtronic Perfusion Systems - 2014-02-12](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/62e1a360-9c5f-46eb-9f56-138156b2b2ae) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2014
- [FDA Inspection 831904 - Medtronic Perfusion Systems - 2013-04-01](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/ec64459e-d450-41ca-a661-d272e3edd3d5) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2013
- [FDA Inspection 831904 - Medtronic Perfusion Systems - 2013-04-01](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/889720c1-ac45-443c-ae0f-57f250dad3f6) — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2013
- [FDA Inspection 764709 - Medtronic Perfusion Systems - 2012-01-23](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/f437580c-6db0-400d-9f2a-b5d03372ed39) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2012
- [FDA Inspection 764709 - Medtronic Perfusion Systems - 2012-01-23](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/abb623ec-00ee-4c1b-8e61-2824c45b9f7f) — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2012
- [FDA Inspection 667045 - Medtronic Perfusion Systems - 2010-06-15](https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/19c7b511-a3e8-4699-83e5-50266b07aaf5) — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2010

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