# FDA Inspection 1111959 - Qualitel Corporation - December 05, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/qualitel-corporation/0c27f1d2-3a74-4335-a6ad-a4ed76bb8d4a
Source feed: FDA_Inspections

> FDA Inspection 1111959 for Qualitel Corporation on December 05, 2019. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1111959
- Company Name: Qualitel Corporation
- Inspection Date: 2019-12-05
- 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 1111959 - 2019-12-05](https://www.globalkeysolutions.net/records/fda_inspections/qualitel-corporation/1577e90e-0970-4da2-8425-9b26a3a9fac2)
- [FDA Inspection 959747 - 2016-01-05](https://www.globalkeysolutions.net/records/fda_inspections/qualitel-corporation/d65aa3a7-423f-4a46-b957-a9094dbc4525)
- [FDA Inspection 959747 - 2016-01-05](https://www.globalkeysolutions.net/records/fda_inspections/qualitel-corporation/cde464af-90f8-43ec-93e2-1afa0e0c65da)
- [FDA Inspection 863787 - 2014-01-27](https://www.globalkeysolutions.net/records/fda_inspections/qualitel-corporation/664f1d06-6365-403a-b239-e1be59e65d00)
- [FDA Inspection 790097 - 2012-06-29](https://www.globalkeysolutions.net/records/fda_inspections/qualitel-corporation/dd80bf36-91ee-40ff-81a4-ba392651b5c5)

Company: https://www.globalkeysolutions.net/companies/qualitel-corporation/43b702fc-1bd7-4869-8675-d96d02b784a0

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