FDA Inspection 1032404 - Stryker Neurovascular - September 22, 2017

Record Details

This FDA Inspection record concerns Stryker Neurovascular, with an inspection on September 22, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Stryker Neurovascular
Inspection Date: September 22, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c6beae55-269c-4205-8729-bf789ad711d1