# FDA Inspection 749485 - WuJiang City ShenLing Medical Device Co., Ltd. - September 01, 2011

Source: https://www.keypedia.com/records/fda_inspections/wujiang-city-shenling-medical-device-co-ltd/53290e56-87da-43af-b1ee-208a1f9136c0
Source feed: FDA_Inspections

> FDA Inspection 749485 for WuJiang City ShenLing Medical Device Co., Ltd. on September 01, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 749485
- Company Name: WuJiang City ShenLing Medical Device Co., Ltd.
- Inspection Date: 2011-09-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 923293 - 2015-03-19](https://www.keypedia.com/records/fda_inspections/wujiang-city-shenling-medical-device-co-ltd/d64ef5fc-fdda-47e0-81d4-e45af567584f)

Company: https://www.keypedia.com/companies/wujiang-city-shenling-medical-device-co-ltd/92ea1376-0a3c-41da-9944-0bbf5e4b0e3e

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