FDA Inspection 992239 - Medtronic Vascular Galway DBA Medtronic Ireland - October 27, 2016

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Record Details

This FDA Inspection record concerns Medtronic Vascular Galway DBA Medtronic Ireland, with an inspection on October 27, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Vascular Galway DBA Medtronic Ireland
Inspection Date: October 27, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 30435f9d-1c6b-481c-a713-e95f94f59059