# Guangzhou Sunine Laser Technology Co. Ltd. – FDA Inspection, Dec 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/guangzhou-sunine-laser-technology-co-ltd/d5664489-33e6-4840-a376-7839335be581
Source feed: FDA_Inspections

> FDA inspection 1046760 of Guangzhou Sunine Laser Technology Co. Ltd., December 01, 2017. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046760
- Company Name: Guangzhou Sunine Laser Technology Co. Ltd.
- Inspection Date: 2017-12-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1295984 - 2025-05-26

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/emir-galevi/d99d0e13-df64-44a8-af6e-ef28ff50b5b9)
- Issuing Officer

Company: https://www.keypedia.com/companies/guangzhou-sunine-laser-technology-co-ltd/75412bfa-9176-4886-82fb-bab27e4e9469

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