# DK MEDICAL SYSTEMS CO., LTD. – FDA Inspection, Nov 2, 2023

Source: https://www.keypedia.com/records/fda_inspections/dk-medical-systems-co-ltd/9bc1a502-c070-4800-9a88-12f1b1a07b02
Source feed: FDA_Inspections

> FDA inspection 1223665 of DK MEDICAL SYSTEMS CO., LTD., November 02, 2023. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1223665
- Company Name: DK MEDICAL SYSTEMS CO., LTD.
- Inspection Date: 2023-11-02
- 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: 10

## Related Documents

- [FDA Inspection 1335994 - 2026-09-17](https://www.keypedia.com/records/fda_inspections/dk-medical-systems-co-ltd/a4455728-4489-40b2-b195-6d37681505a7)

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/dk-medical-systems-co-ltd/7f4c670e-4272-47d8-8fce-70e1bfe51dda

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