# FDA Inspection 923737 - Shenzhen Rekelaser Technology Co. Ltd. - November 20, 2014

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-rekelaser-technology-co-ltd/34d01fed-f471-43ea-acef-7d811da0309e
Source feed: FDA_Inspections

> FDA Inspection 923737 for Shenzhen Rekelaser Technology Co. Ltd. on November 20, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 923737
- Company Name: Shenzhen Rekelaser Technology Co. Ltd.
- Inspection Date: 2014-11-20
- 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-rekelaser-technology-co-ltd/bcd7979b-594e-4092-b6e7-480448622125

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