# CG MedTech Co., Ltd. – FDA Inspection, Jun 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/cg-medtech-co-ltd/94705ef1-9b69-48cf-b6ba-582bf9c9fd0d
Source feed: FDA_Inspections

> FDA inspection 1209400 of CG MedTech Co., Ltd., June 15, 2023. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 806 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1209400
- Company Name: CG MedTech Co., Ltd.
- Inspection Date: 2023-06-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- [FDA Inspection 1327740 - 2026-09-10](https://www.keypedia.com/records/fda_inspections/cg-medtech-co-ltd/be37fc35-a946-44e0-8a7f-9ce7821f0138)
- FDA Inspection 1112977 - 2019-11-14
- FDA Inspection 1023511 - 2017-03-30
- [FDA Inspection 922594 - 2015-02-05](https://www.keypedia.com/records/fda_inspections/cg-medtech-co-ltd/a0fab345-09b1-4a0e-8bc9-280b7d2e4eea)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/karen-m-cruz-arenas/6c698301-84ca-4ba7-a79c-309721db2f1b)

Company: https://www.keypedia.com/companies/cg-medtech-co-ltd/3b0b9840-df4f-48ee-af93-2fc9eb4cc05f

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