# CG MedTech Co. Ltd – FDA Inspection, Sep 11, 2025

Source: https://www.keypedia.com/records/fda_inspections/cg-medtech-co-ltd/d617aa18-c263-4e86-89aa-63f29d1e9dd6
Source feed: FDA_Inspections

> FDA inspection 1281106 of CG MedTech Co. Ltd, September 11, 2025. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1281106
- Company Name: CG MedTech Co. Ltd
- Inspection Date: 2025-09-11
- 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: 2

## Related Documents

- FDA Inspection 1341056 - 2026-09-08
- [FDA Inspection 966649 - 2016-03-25](https://www.keypedia.com/records/fda_inspections/cg-medtech-co-ltd/2f2ba719-cc46-4cad-b92e-04be56e6754f)
- FDA Inspection 620307 - 2009-09-25

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/cg-medtech-co-ltd/ad3399fe-fe3f-4a17-a987-f3c21755997c

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