# DT MedTech, LLC – FDA Inspection, Oct 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/dt-medtech-llc/fb9f2a0f-4dd2-4bf0-80c1-ecdb41584381
Source feed: FDA_Inspections

> FDA inspection 1029760 of DT MedTech, LLC, October 24, 2017. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029760
- Company Name: DT MedTech, LLC
- Inspection Date: 2017-10-24
- 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: 4

## Related Documents

- [FDA Inspection 1319492 - 2026-05-28](https://www.keypedia.com/records/fda_inspections/dt-medtech-llc/55ff8cbc-d25d-4d9a-8a44-aae5212d11c6)
- [FDA Inspection 991573 - 2016-11-08](https://www.keypedia.com/records/fda_inspections/dt-medtech-llc/2d3da50b-012c-410a-bc11-413797d30f06)

## Related Officers

- Issuing Officer
- [Company Rep](https://www.keypedia.com/people/james-m-simpson/3c0113ae-d846-4e37-aafa-13d58c465fa3)
- [Issuing Officer](https://www.keypedia.com/people/katelyn-a-staub-zamperini/bb7f95a4-53c1-473c-856e-517312bdba30)

Company: https://www.keypedia.com/companies/dt-medtech-llc/0f6b0f0f-322c-4b5c-a5dc-500309b79ce4

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