# FDA Inspection 1172372 - Knox Medical Diagnostics, Inc. - June 21, 2022

Source: https://www.globalkeysolutions.net/records/fda_inspections/knox-medical-diagnostics-inc/670c0071-1e8d-4255-b1c8-5e5eb86f5abd
Source feed: FDA_Inspections

> FDA Inspection 1172372 for Knox Medical Diagnostics, Inc. on June 21, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1172372
- Company Name: Knox Medical Diagnostics, Inc.
- Inspection Date: 2022-06-21
- 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 1247227 - 2024-08-21](https://www.globalkeysolutions.net/records/fda_inspections/knox-medical-diagnostics-inc/81773866-0c90-41b4-8b46-0fc6d03adf35)
- [FDA Inspection 1247227 - 2024-08-21](https://www.globalkeysolutions.net/records/fda_inspections/knox-medical-diagnostics-inc/afd3229b-790e-415b-a863-5a692ec37626)
- [FDA Inspection 1172372 - 2022-06-21](https://www.globalkeysolutions.net/records/fda_inspections/knox-medical-diagnostics-inc/210bacf3-5d4a-4784-b4f8-6c3c2822b862)

Company: https://www.globalkeysolutions.net/companies/knox-medical-diagnostics-inc/57ec58a9-edf8-40be-89a3-401969e27047

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