FDA Inspection 1028734 - Stryker Neurovascular - October 16, 2017

Record Details

This FDA Inspection record concerns Stryker Neurovascular, with an inspection on October 16, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Stryker Neurovascular
Inspection Date: October 16, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 830feb26-c340-4730-a20c-71c55f4e6fc9