# FDA Inspection 1026106 - STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD. - August 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/stryker-suzhou-medical-technology-co-ltd/498c9423-641d-485d-8296-f89f0af48b8e
Source feed: FDA_Inspections

> FDA Inspection 1026106 for STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD. on August 24, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026106
- Company Name: STRYKER (SUZHOU) MEDICAL TECHNOLOGY CO., LTD.
- Inspection Date: 2017-08-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 903664 - 2014-10-29](https://www.keypedia.com/records/fda_inspections/stryker-suzhou-medical-technology-co-ltd/415b91f3-8978-4b0c-a028-a380e74868f2)

Company: https://www.keypedia.com/companies/stryker-suzhou-medical-technology-co-ltd/fac3a357-f220-40ec-ba43-3d117ab2280a

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