# Knox Medical Diagnostics, Inc. – FDA Inspection, Aug 21, 2024

Source: https://www.keypedia.com/records/fda_inspections/knox-medical-diagnostics-inc/afd3229b-790e-415b-a863-5a692ec37626
Source feed: FDA_Inspections

> FDA inspection 1247227 of Knox Medical Diagnostics, Inc., August 21, 2024. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1247227
- Company Name: Knox Medical Diagnostics, Inc.
- Inspection Date: 2024-08-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1172372 - 2022-06-21](https://www.keypedia.com/records/fda_inspections/knox-medical-diagnostics-inc/670c0071-1e8d-4255-b1c8-5e5eb86f5abd)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/alex-j-wild/bb1b66b3-19b9-480e-af0b-f06f8de0d930)
- [Investigator](https://www.keypedia.com/people/nga-t-ho/7c7d96a2-9b2c-4966-8dc2-ee20ca024be1)

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

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