# FDA Inspection 586860 - Stryker Spine - May 28, 2009

Source: https://www.keypedia.com/records/fda_inspections/stryker-spine/bf8ad005-affa-4a54-a1c1-d6a55cd42a96
Source feed: FDA_Inspections

> FDA Inspection 586860 for Stryker Spine on May 28, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 586860
- Company Name: Stryker Spine
- Inspection Date: 2009-05-28
- 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 1257920 - 2024-12-12](https://www.keypedia.com/records/fda_inspections/stryker-spine/6df3afb5-95ae-4aca-97be-5d3adb4ddca2)
- [FDA Inspection 1257920 - 2024-12-12](https://www.keypedia.com/records/fda_inspections/stryker-spine/17484b9f-e2c1-4f5b-8625-a12b8da939e1)
- [FDA Inspection 1257920 - 2024-12-12](https://www.keypedia.com/records/fda_inspections/stryker-spine/59b85a18-2780-487f-90bf-f3439e4cd7f3)
- [FDA Inspection 966647 - 2016-02-10](https://www.keypedia.com/records/fda_inspections/stryker-spine/21a12f8e-e57d-4f6d-8072-0c96f9fd4183)
- [FDA Inspection 966647 - 2016-02-10](https://www.keypedia.com/records/fda_inspections/stryker-spine/9d8b574e-784d-4113-8144-c38b238a6854)

Company: https://www.keypedia.com/companies/stryker-spine/6cfbb80a-1ad5-4c55-90f8-8487e747b60c

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