# FDA Inspection 1019784 - Beijing Syntech Laser Co., Ltd - July 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/beijing-syntech-laser-co-ltd/a73dee04-4fc2-41cb-aee3-e2794f61ba03
Source feed: FDA_Inspections

> FDA Inspection 1019784 for Beijing Syntech Laser Co., Ltd on July 07, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019784
- Company Name: Beijing Syntech Laser Co., Ltd
- Inspection Date: 2017-07-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1019784 - 2017-07-07](https://www.keypedia.com/records/fda_inspections/beijing-syntech-laser-co-ltd/190cd0d9-90f1-41ed-9e57-0a63f9d6e75a)
- [FDA Inspection 841544 - 2013-07-12](https://www.keypedia.com/records/fda_inspections/beijing-syntech-laser-co-ltd/9690537d-9217-4271-a69f-029fcbd2c530)
- [FDA Inspection 841544 - 2013-07-12](https://www.keypedia.com/records/fda_inspections/beijing-syntech-laser-co-ltd/5ad923f9-fcbf-4885-8528-d059758a4770)
- [FDA Inspection 841544 - 2013-07-12](https://www.keypedia.com/records/fda_inspections/beijing-syntech-laser-co-ltd/595ff68d-37e8-457f-9f29-f9f8bd635c53)

Company: https://www.keypedia.com/companies/beijing-syntech-laser-co-ltd/490082ac-bf8e-4e21-99bb-a16c34519ccf

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