# FDA Inspection 1089422 - Beijing Sundor Laser Equipment Co. Ltd. - November 09, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/beijing-sundor-laser-equipment-co-ltd/b086c97b-a9a0-4c48-8ac9-830275d0c8a2
Source feed: FDA_Inspections

> FDA Inspection 1089422 for Beijing Sundor Laser Equipment Co. Ltd. on November 09, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089422
- Company Name: Beijing Sundor Laser Equipment Co. Ltd.
- Inspection Date: 2018-11-09
- 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/beijing-sundor-laser-equipment-co-ltd/07891f20-93dd-4c94-bfd8-2e71f7bec3fc

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