# FDA Inspection 1244901 - Imedrix Inc - July 24, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/imedrix-inc/03deb29b-c439-4deb-a01e-e88f3172b1d8
Source feed: FDA_Inspections

> FDA Inspection 1244901 for Imedrix Inc on July 24, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1244901
- Company Name: Imedrix Inc
- Inspection Date: 2024-07-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1244901 - 2024-07-24](https://www.globalkeysolutions.net/records/fda_inspections/imedrix-inc/1688e8c8-bf2d-45b1-9aa2-991d0cdfc960)
- [FDA Inspection 1190350 - 2022-11-04](https://www.globalkeysolutions.net/records/fda_inspections/imedrix-inc/833da7ce-4d12-456e-b93d-1aaf28570b13)

Company: https://www.globalkeysolutions.net/companies/imedrix-inc/2b33c6fa-e527-4422-a192-e2fb3a6cdf6a

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