# FDA Inspection 1026794 - Sunny Medical Device (Shenzhen) Co., Ltd. - August 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/sunny-medical-device-shenzhen-co-ltd/9109e99e-a48a-4d65-be03-92cc4ce5d506
Source feed: FDA_Inspections

> FDA Inspection 1026794 for Sunny Medical Device (Shenzhen) Co., Ltd. on August 17, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026794
- Company Name: Sunny Medical Device (Shenzhen) Co., Ltd.
- Inspection Date: 2017-08-17
- 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 1026794 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/sunny-medical-device-shenzhen-co-ltd/3edcf6e8-f7b4-40f2-8af5-0752ec4bc5c2)

Company: https://www.keypedia.com/companies/sunny-medical-device-shenzhen-co-ltd/6c2ea693-3900-49f7-ad3b-b61fb878c492

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