FDA Inspection
Howmedica Osteonics Corp dba Stryker CraniomaxillofacialFDA Inspection 619849 - Howmedica Osteonics Corp dba Stryker Craniomaxillofacial - September 30, 2009
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Record Details
This FDA Inspection record concerns Howmedica Osteonics Corp dba Stryker Craniomaxillofacial, with an inspection on September 30, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- September 30, 2009
- Product Type
- Devices
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ID · 13001547-34fc-499d-ac8a-ce17b3484507