# Canwell Medical Co. Ltd. – FDA Inspection, Feb 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/canwell-medical-co-ltd/ad511fdf-c52f-499d-8a0e-999790933bb8
Source feed: FDA_Inspections

> FDA inspection 1009911 of Canwell Medical Co. Ltd., February 23, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009911
- Company Name: Canwell Medical Co. Ltd.
- Inspection Date: 2017-02-23
- 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

- [FDA Associated Person](https://www.keypedia.com/people/joseph-r-strelnik/1fb7d50e-abf2-45ef-85a8-71c61b33e42d)

Company: https://www.keypedia.com/companies/canwell-medical-co-ltd/06aacf6d-c985-4585-8eb9-597fbb966d42

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