# FDA Inspection 883815 - Suzhou Weikang Medical Apparatus Co., Ltd. - May 29, 2014

Source: https://www.keypedia.com/records/fda_inspections/suzhou-weikang-medical-apparatus-co-ltd/01cc3c8f-9503-448a-ad0d-deeffbef0c0c
Source feed: FDA_Inspections

> FDA Inspection 883815 for Suzhou Weikang Medical Apparatus Co., Ltd. on May 29, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 883815
- Company Name: Suzhou Weikang Medical Apparatus Co., Ltd.
- Inspection Date: 2014-05-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 704358 - 2010-12-16](https://www.keypedia.com/records/fda_inspections/suzhou-weikang-medical-apparatus-co-ltd/1b9cd915-bf31-4820-a233-cc25628f34d6)

Company: https://www.keypedia.com/companies/suzhou-weikang-medical-apparatus-co-ltd/4275efb2-2880-4966-a317-2f81963727d8

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