# FDA Inspection 1079767 - Kaesung Co., Ltd. - January 24, 2019

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

> FDA Inspection 1079767 for Kaesung Co., Ltd. on January 24, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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