# FDA Inspection 729867 - Howmedica Osteonics Corp dba Stryker Craniomaxillofacial - May 20, 2011

Source: https://www.keypedia.com/records/fda_inspections/howmedica-osteonics-corp-dba-stryker-craniomaxillofacial/2adebcb1-4561-47b9-9c74-a185bac4aa66
Source feed: FDA_Inspections

> FDA Inspection 729867 for Howmedica Osteonics Corp dba Stryker Craniomaxillofacial on May 20, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 729867
- Company Name: Howmedica Osteonics Corp dba Stryker Craniomaxillofacial
- Inspection Date: 2011-05-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 729867 - 2011-05-20](https://www.keypedia.com/records/fda_inspections/howmedica-osteonics-corp-dba-stryker-craniomaxillofacial/59079f01-fb37-48a1-ae47-749e66827794)
- [FDA Inspection 619849 - 2009-09-30](https://www.keypedia.com/records/fda_inspections/howmedica-osteonics-corp-dba-stryker-craniomaxillofacial/13001547-34fc-499d-ac8a-ce17b3484507)
- [FDA Inspection 619849 - 2009-09-30](https://www.keypedia.com/records/fda_inspections/howmedica-osteonics-corp-dba-stryker-craniomaxillofacial/e6ddeef0-2879-4747-b19f-afc3ff179cfe)

Company: https://www.keypedia.com/companies/howmedica-osteonics-corp-dba-stryker-craniomaxillofacial/dccee19b-686c-4b60-9a27-123fabc0861e

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