FDA Inspection 1030805 - Medtronic Sofamor Danek USA, Inc - October 26, 2017

Record Details

This FDA Inspection record concerns Medtronic Sofamor Danek USA, Inc, with an inspection on October 26, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Medtronic Sofamor Danek USA, Inc
Inspection Date: October 26, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a291e243-052d-491c-b74f-502e2db0d04a