# DE TECH CO.,LTD – FDA Inspection, Jul 27, 2023

Source: https://www.keypedia.com/records/fda_inspections/de-tech-coltd/ae2cfe17-35be-47e0-9e40-960b3fe6f26f
Source feed: FDA_Inspections

> FDA inspection 1214470 of DE TECH CO.,LTD, July 27, 2023. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1214470
- Company Name: DE TECH CO.,LTD
- Inspection Date: 2023-07-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/christina-l-bigham/f3da8e26-4a8c-43a8-8070-349fe4500289)

Company: https://www.keypedia.com/companies/de-tech-coltd/2fd8e4bc-e789-4fee-b4c5-e2e26985a15f

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