# FDA Inspection 938710 - Stryker Medtech K.K. - July 16, 2015

Source: https://www.keypedia.com/records/fda_inspections/stryker-medtech-kk/d136b834-e408-4dda-8ada-609ad2d05c9a
Source feed: FDA_Inspections

> FDA Inspection 938710 for Stryker Medtech K.K. on July 16, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938710
- Company Name: Stryker Medtech K.K.
- Inspection Date: 2015-07-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 938710 - 2015-07-16](https://www.keypedia.com/records/fda_inspections/stryker-medtech-kk/767682ec-764e-42a0-a936-1cb3d9acd6f5)

Company: https://www.keypedia.com/companies/stryker-medtech-kk/09ab905e-b4b3-4889-bfa1-25eac6940656

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