FDA Inspection 823591 - Medtronic Vascular Galway DBA Medtronic Ireland - March 22, 2013

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Record Details

This FDA Inspection record concerns Medtronic Vascular Galway DBA Medtronic Ireland, with an inspection on March 22, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Vascular Galway DBA Medtronic Ireland
Inspection Date: March 22, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9ab38831-afa2-4cda-83cc-9929e081427c