# FDA Inspection 1102021 - BIAOKE LASER TECHNOLOGY (HANGZHOU) CO., LTD. - May 30, 2019

Source: https://www.keypedia.com/records/fda_inspections/biaoke-laser-technology-hangzhou-co-ltd/5c2d9401-840d-4fbe-8e22-2724a851fc64
Source feed: FDA_Inspections

> FDA Inspection 1102021 for BIAOKE LASER TECHNOLOGY (HANGZHOU) CO., LTD. on May 30, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102021
- Company Name: BIAOKE LASER TECHNOLOGY (HANGZHOU) CO., LTD.
- Inspection Date: 2019-05-30
- Classification: Voluntary Action Indicated (VAI)
- 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/biaoke-laser-technology-hangzhou-co-ltd/0b04a238-b70b-4671-b061-ab834d2130e2

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