# FDA Inspection 1227125 - QFIX - October 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/qfix/91c2bba6-8517-4bca-bf39-23cbf0d09563
Source feed: FDA_Inspections

> FDA Inspection 1227125 for QFIX on October 20, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1227125
- Company Name: QFIX
- Inspection Date: 2023-10-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1227125 - 2023-10-20](https://www.keypedia.com/records/fda_inspections/qfix/6212ddd5-9b98-4a24-a284-44a927b85614)
- [FDA Inspection 1227125 - 2023-10-20](https://www.keypedia.com/records/fda_inspections/qfix/f11d8b4c-accd-4e72-8577-9296b99b2412)
- [FDA Inspection 1069651 - 2018-09-24](https://www.keypedia.com/records/fda_inspections/qfix/93906473-d5f8-4a75-9284-48ef5d412063)

Company: https://www.keypedia.com/companies/qfix/b7c33d98-43e9-42f9-998c-958aa9e92986

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