# FDA Inspection 1065602 - SHENZHEN TSD LASER EQUIPMENT CO., LTD. - December 06, 2017

Source: https://www.keypedia.com/records/fda_inspections/shenzhen-tsd-laser-equipment-co-ltd/17d218ce-46a3-4279-89b5-599e3509928b
Source feed: FDA_Inspections

> FDA Inspection 1065602 for SHENZHEN TSD LASER EQUIPMENT CO., LTD. on December 06, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065602
- Company Name: SHENZHEN TSD LASER EQUIPMENT CO., LTD.
- Inspection Date: 2017-12-06
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1218698 - 2023-08-30](https://www.keypedia.com/records/fda_inspections/shenzhen-tsd-laser-equipment-co-ltd/7017ce9b-927e-4689-9fc8-0d2cfde0678d)

Company: https://www.keypedia.com/companies/shenzhen-tsd-laser-equipment-co-ltd/ea817a45-420a-47fa-b828-0b38c1a8ca81

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