# QFIX – FDA Inspection, Oct 20, 2023

Source: https://www.keypedia.com/records/fda_inspections/qfix/f11d8b4c-accd-4e72-8577-9296b99b2412
Source feed: FDA_Inspections

> FDA inspection 1227125 of QFIX, October 20, 2023. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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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)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1069651 - 2018-09-24

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/edward-d-mcdonald/69224613-2b96-426a-99dd-e1cfe5ff1713)

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