# FDA Inspection 987886 - Meixin Medical Suzhou Co., Ltd. - April 28, 2016

Source: https://www.keypedia.com/records/fda_inspections/meixin-medical-suzhou-co-ltd/1143162e-7b7c-441f-b5c4-6d9de84a3042
Source feed: FDA_Inspections

> FDA Inspection 987886 for Meixin Medical Suzhou Co., Ltd. on April 28, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 987886
- Company Name: Meixin Medical Suzhou Co., Ltd.
- Inspection Date: 2016-04-28
- 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 987886 - 2016-04-28](https://www.keypedia.com/records/fda_inspections/meixin-medical-suzhou-co-ltd/7979e7aa-b322-4a63-9207-a56ec907cd93)
- [FDA Inspection 812189 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/meixin-medical-suzhou-co-ltd/a09d73cd-17a7-43ce-8e4c-2ae6e0450fad)
- [FDA Inspection 812189 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/meixin-medical-suzhou-co-ltd/7ea877bd-354d-4131-bcaf-f2517765e265)

Company: https://www.keypedia.com/companies/meixin-medical-suzhou-co-ltd/7ebb6628-1683-4249-ab68-d9472bdf1d6b

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