# FDA Inspection 991573 - DT MedTech, LLC - November 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/dt-medtech-llc/c1c084cc-e24e-4c24-af23-adeb3c466bf0
Source feed: FDA_Inspections

> FDA Inspection 991573 for DT MedTech, LLC on November 08, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 991573
- Company Name: DT MedTech, LLC
- Inspection Date: 2016-11-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1029760 - 2017-10-24](https://www.keypedia.com/records/fda_inspections/dt-medtech-llc/fb9f2a0f-4dd2-4bf0-80c1-ecdb41584381)

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