# FDA Inspection 597734 - Stryker Imaging - July 20, 2009

Source: https://www.keypedia.com/records/fda_inspections/stryker-imaging/3709fa17-c6a2-4a85-9613-0f61c80263ab
Source feed: FDA_Inspections

> FDA Inspection 597734 for Stryker Imaging on July 20, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 597734
- Company Name: Stryker Imaging
- Inspection Date: 2009-07-20
- 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 597734 - 2009-07-20](https://www.keypedia.com/records/fda_inspections/stryker-imaging/c3978848-fc90-4637-afbe-fa37ba371540)

Company: https://www.keypedia.com/companies/stryker-imaging/06f52d3c-cf45-4389-ac21-95953dcb6168

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