# FDA Inspection 1054301 - Shenzhen Henglitian Technology Co. Ltd. - December 11, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/shenzhen-henglitian-technology-co-ltd/1ae208bd-4cbe-4f9a-9197-7c97561564cc
Source feed: FDA_Inspections

> FDA Inspection 1054301 for Shenzhen Henglitian Technology Co. Ltd. on December 11, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1054301
- Company Name: Shenzhen Henglitian Technology Co. Ltd.
- Inspection Date: 2017-12-11
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.globalkeysolutions.net/companies/shenzhen-henglitian-technology-co-ltd/fe5f265f-f498-4b82-b8ef-0c4fdf731ff6

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