# FDA Inspection 617466 - Tae Yeon Medical Co Ltd - September 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/tae-yeon-medical-co-ltd/8ff221c6-ffc8-4809-a014-b2ff4e6f02d3
Source feed: FDA_Inspections

> FDA Inspection 617466 for Tae Yeon Medical Co Ltd on September 24, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 617466
- Company Name: Tae Yeon Medical Co Ltd
- Inspection Date: 2009-09-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/tae-yeon-medical-co-ltd/ee9b1e9d-589b-4b72-800a-ae7db044a2b1

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