# FDA Inspection 1029760 - DT MedTech, LLC - October 24, 2017

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

> FDA Inspection 1029760 for DT MedTech, LLC on October 24, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 991573 - 2016-11-08](https://www.globalkeysolutions.net/api/records/fda_inspections/dt-medtech-llc/c1c084cc-e24e-4c24-af23-adeb3c466bf0/)

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

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