# FDA Inspection 1174991 - FABRITEQ LLC - June 14, 2022

Source: https://www.keypedia.com/records/fda_inspections/fabriteq-llc/467b7ae0-c786-4e61-91de-58616c5a37d9
Source feed: FDA_Inspections

> FDA Inspection 1174991 for FABRITEQ LLC on June 14, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1174991
- Company Name: FABRITEQ LLC
- Inspection Date: 2022-06-14
- 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 1174991 - 2022-06-14](https://www.keypedia.com/records/fda_inspections/fabriteq-llc/3c13fae9-a599-4ef2-b861-ee018ed97e4c)
- [FDA Inspection 1031306 - 2017-11-01](https://www.keypedia.com/records/fda_inspections/fabriteq-llc/b7262890-be04-425c-bb4e-09f8c5fcae30)
- [FDA Inspection 1031306 - 2017-11-01](https://www.keypedia.com/records/fda_inspections/fabriteq-llc/07730932-21d7-4df7-a216-5c4e848bc841)

Company: https://www.keypedia.com/companies/fabriteq-llc/1389a7e4-3c99-46e6-84b5-be7819b438e2

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