# FDA Inspection 1058725 - Shenzhen Viatom Technology Co., Ltd. - February 07, 2018

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-viatom-technology-co-ltd/e4115213-ab4a-4dca-a3ce-fe47bbf8e0ec
Source feed: FDA_Inspections

> FDA Inspection 1058725 for Shenzhen Viatom Technology Co., Ltd. on February 07, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1058725
- Company Name: Shenzhen Viatom Technology Co., Ltd.
- Inspection Date: 2018-02-07
- 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 1058725 - 2018-02-07](https://www.keypedia.com/records/fda_inspections/shenzhen-viatom-technology-co-ltd/99a64b9c-b309-4bb4-aa85-48c065e95ff7)

Company: https://www.keypedia.com/companies/shenzhen-viatom-technology-co-ltd/d78a489c-852d-42a6-9072-b39f3e8057da

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