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FDA Inspection
•Medtronic Perfusion Systems•September 30, 2016

FDA Inspection 987452 - Medtronic Perfusion Systems - September 30, 2016

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Record Details

This FDA Inspection record concerns Medtronic Perfusion Systems, with an inspection on September 30, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company
Medtronic Perfusion Systems
Inspection Date
September 30, 2016
Product Type
Devices
Office
Center for Devices and Radiological Health
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ID · 824b6add-4362-4992-9175-dec9fc4a088f

Violation Codes4
21 CFR 803.50(a)(2)21 CFR 820.100(a)21 CFR 820.198(c)21 CFR 820.30(g)

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