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

Source: https://www.globalkeysolutions.net/records/fda_inspections/stryker-craniomaxillofacial-division/e6b4c1ba-b53d-4deb-93c4-67209ac241e0
Source feed: FDA_Inspections

> FDA Inspection 551446 for Stryker Craniomaxillofacial Division on December 10, 2008. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 551446
- Company Name: Stryker Craniomaxillofacial Division
- Inspection Date: 2008-12-10
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 674776 - 2010-08-02](https://www.globalkeysolutions.net/records/fda_inspections/stryker-craniomaxillofacial-division/07d3a471-5887-47a3-8808-925e21830ddd)
- [FDA Inspection 551446 - 2008-12-10](https://www.globalkeysolutions.net/records/fda_inspections/stryker-craniomaxillofacial-division/494635dd-c090-41c9-909d-06d7549d9421)

Company: https://www.globalkeysolutions.net/companies/stryker-craniomaxillofacial-division/920c1df1-ec95-4c6a-948a-3f6f4297c5c5

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7