# BEIJING TAIKESIMAN TECHNOLOGY DEVELOPMENT CO., LTD – FDA Inspection, Jan 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/beijing-taikesiman-technology-development-co-ltd/1b45250b-c606-4c89-af5b-2c8356f51357
Source feed: FDA_Inspections

> FDA inspection 1008390 of BEIJING TAIKESIMAN TECHNOLOGY DEVELOPMENT CO., LTD, January 13, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008390
- Company Name: BEIJING TAIKESIMAN TECHNOLOGY DEVELOPMENT CO., LTD
- Inspection Date: 2017-01-13
- 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: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/mark-e-chan/2a5a3abf-96f6-4ceb-b87d-379ed5c6f47e)

Company: https://www.keypedia.com/companies/beijing-taikesiman-technology-development-co-ltd/9bbc7080-30cf-4575-b493-cf70914996de

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