FDA establishment 3016721526, San Francisco, California, United States. Part of Knox Medical Diagnostics's FDA records. Every inspection FDA has posted for the site, with its outcome and cited regulations.
FY2018 to FY2027 to date; 0 classified OAI
A hatched bar is a year that is not over, so its count covers only part of the year.
Inspections citing each reference
| Ended | Product and area | Citations | Classification |
|---|---|---|---|
| Aug 21, 2024 | Devices · Postmarket Assurance: DevicesDevices · Compliance: Devices | 2 cited references
| Voluntary Action Indicated (VAI) |
| Jun 21, 2022 | Devices · Postmarket Assurance: DevicesDevices · Compliance: Devices | 1 cited reference
| No Action Indicated (NAI) |
An FEI (FDA Establishment Identifier) names one physical site. Inspections, outcomes and citations come from FDA's Data Dashboard; FDA posts citations only for some inspections. A contract site can make products for many companies, so the company shown is the one FDA lists as the site's firm. FDA Data Dashboard and warning letters
San Francisco, California, United States. Part of