# Medtronic Perfusion Systems – FDA Inspection, Sep 30, 2016

Source: https://www.keypedia.com/records/fda_inspections/medtronic-perfusion-systems/824b6add-4362-4992-9175-dec9fc4a088f
Source feed: FDA_Inspections

> FDA inspection 987452 of Medtronic Perfusion Systems, September 30, 2016. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 7 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987452
- Company Name: Medtronic Perfusion Systems
- Inspection Date: 2016-09-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1178299 - 2022-06-23
- FDA Inspection 886720 - 2014-06-24
- FDA Inspection 867900 - 2014-02-12
- FDA Inspection 831904 - 2013-04-01
- FDA Inspection 764709 - 2012-01-23

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