# FDA Inspection 559235 - Medtronic Perfusion Systems - January 23, 2009

Source: https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/074cf177-e39d-466e-b13d-e962d7908e4f
Source feed: FDA_Inspections

> FDA Inspection 559235 for Medtronic Perfusion Systems on January 23, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 559235
- Company Name: Medtronic Perfusion Systems
- Inspection Date: 2009-01-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7