# Beijing Syntech Laser Co., Ltd – FDA Inspection, Jul 7, 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 of Beijing Syntech Laser Co., Ltd, July 07, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 820, 1002 and 1010. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 841544 - 2013-07-12](https://www.keypedia.com/records/fda_inspections/beijing-syntech-laser-co-ltd/9690537d-9217-4271-a69f-029fcbd2c530)

## Related Officers

- [Investigator](https://www.keypedia.com/people/dawn-m-braswell/6a66fdbb-fff8-4b4b-9f06-320464957b87)

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