# Kaesung Co., Ltd. – FDA Inspection, Jan 24, 2019

Source: https://www.keypedia.com/records/fda_inspections/kaesung-co-ltd/2cda1b36-e284-4ab5-93c7-e52b525c3432
Source feed: FDA_Inspections

> FDA inspection 1079767 of Kaesung Co., Ltd., January 24, 2019. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079767
- Company Name: Kaesung Co., Ltd.
- Inspection Date: 2019-01-24
- 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

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/kaesung-co-ltd/d7a40154-219b-4938-8214-a78212f0d20a

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