# Vortran Medical Technology 1, Inc – FDA Inspection, Apr 11, 2017

Source: https://www.keypedia.com/records/fda_inspections/vortran-medical-technology-1-inc/b2692bbc-45ae-4184-ac2d-5105109a8cc3
Source feed: FDA_Inspections

> FDA inspection 1010791 of Vortran Medical Technology 1, Inc, April 11, 2017. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 806 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010791
- Company Name: Vortran Medical Technology 1, Inc
- Inspection Date: 2017-04-11
- 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: 10

## Related Documents

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- [FDA Inspection 834679 - 2013-05-29](https://www.keypedia.com/records/fda_inspections/vortran-medical-technology-1-inc/b741d6ed-2fdf-422e-a152-bbcce3c5be1a)
- FDA Inspection 566225 - 2009-02-26

## Related Officers

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

Company: https://www.keypedia.com/companies/vortran-medical-technology-1-inc/15e4ac0e-b666-4e83-a621-32103775cbdf

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