# FDA Inspection 860206 - Feishen Group Co., Ltd. - December 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/feishen-group-co-ltd/bf20256c-c389-4e4c-8dbb-9860327c93f9
Source feed: FDA_Inspections

> FDA Inspection 860206 for Feishen Group Co., Ltd. on December 19, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 860206
- Company Name: Feishen Group Co., Ltd.
- Inspection Date: 2013-12-19
- 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 860206 - 2013-12-19](https://www.keypedia.com/records/fda_inspections/feishen-group-co-ltd/38cc241e-3a28-47b7-8f59-7e7474088c8c)

Company: https://www.keypedia.com/companies/feishen-group-co-ltd/9ffba863-7a4e-4b4a-a580-df46dced1360

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