FDA Inspection
Knox Medical Diagnostics, Inc.Knox Medical Diagnostics, Inc. – FDA Inspection, Aug 21, 2024
Record Details
This FDA Inspection record concerns Knox Medical Diagnostics, Inc., with an inspection on August 21, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · afd3229b-790e-415b-a863-5a692ec37626
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1247227
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
3- 21 CFR 820.198(e)Records of complaint investigation
- 21 CFR 803.18(e)Results of evaluation not in mfr"s MDR file
- 21 CFR 803.18(e)Results of evaluation not in mfr's MDR file
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Other FDA inspections of Knox Medical Diagnostics, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 21, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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