# FDA Inspection 1025096 - SHENZHEN SUNSHINE LASER DEVICES - June 02, 2017

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-sunshine-laser-devices/b1d6ebc2-ff95-43fd-898a-e4101dbac5af
Source feed: FDA_Inspections

> FDA Inspection 1025096 for SHENZHEN SUNSHINE LASER DEVICES on June 02, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025096
- Company Name: SHENZHEN SUNSHINE LASER DEVICES
- Inspection Date: 2017-06-02
- 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.keypedia.com/companies/shenzhen-sunshine-laser-devices/1ce2bab5-77c8-4a4c-b716-67a168f127ef

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