# FDA Inspection 803259 - Shenzhen Layu Laser Technology Co., Ltd. - July 25, 2012

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-layu-laser-technology-co-ltd/9ea48be4-7d75-4c51-acea-93603b9b4ddd
Source feed: FDA_Inspections

> FDA Inspection 803259 for Shenzhen Layu Laser Technology Co., Ltd. on July 25, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803259
- Company Name: Shenzhen Layu Laser Technology Co., Ltd.
- Inspection Date: 2012-07-25
- 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-layu-laser-technology-co-ltd/b1735d6f-1b9c-42d7-a0fd-dd7af3b06a82

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