FDA Inspection 1172372 — Knox Medical Diagnostics, Inc.

Knox Medical Diagnostics, Inc. — FEI 3016721526

The FDA completed an inspection of Knox Medical Diagnostics, Inc. on Jun 21, 2022 in San Francisco, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 21, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Francisco, CA (United States)

Citations

IDCFRDescription
1472221 CFR 820.40Procedures not adequately established or maintained