FDA Inspection 551446 - Stryker Craniomaxillofacial Division - December 10, 2008

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Record Details

This FDA Inspection record concerns Stryker Craniomaxillofacial Division, with an inspection on December 10, 2008, issued by the Center for Devices and Radiological Health, covering devices.

Company: Stryker Craniomaxillofacial Division
Inspection Date: December 10, 2008
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 494635dd-c090-41c9-909d-06d7549d9421