# FDA Inspection 1014723 - Hantel Technologies Inc - June 08, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/hantel-technologies-inc/a809e111-06c9-4aad-8bc1-8c608471f79b
Source feed: FDA_Inspections

> FDA Inspection 1014723 for Hantel Technologies Inc on June 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1014723
- Company Name: Hantel Technologies Inc
- Inspection Date: 2017-06-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 792917 - 2012-07-24](https://www.globalkeysolutions.net/records/fda_inspections/hantel-technologies-inc/da642f9c-229b-4bae-8068-6caabe52ca18)
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Company: https://www.globalkeysolutions.net/companies/hantel-technologies-inc/21311ae5-603e-4d69-a3cb-edfabee85ebc

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