# TaiDoc Technology Corporation – FDA Inspection, Jul 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/taidoc-technology-corporation/f5fa2def-2872-4753-a229-606016e6a323
Source feed: FDA_Inspections

> FDA inspection 1021542 of TaiDoc Technology Corporation, July 13, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021542
- Company Name: TaiDoc Technology Corporation
- Inspection Date: 2017-07-13
- 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 Documents

- [FDA Inspection 1142299 - 2019-08-07](https://www.keypedia.com/records/fda_inspections/taidoc-technology-corporation/82ff2166-dc37-49bc-bb98-32ee8930a669)
- FDA Inspection 868936 - 2014-02-20
- FDA Inspection 732116 - 2011-05-27

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/taidoc-technology-corporation/7df910ba-e12d-493c-8aeb-c44f5e67501f

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