FDA inspection
Knox Medical Diagnostics, Inc.: FDA inspection ending Jun 21, 2022
FDA inspection 1172372 · Voluntary Action Indicated (VAI) · San Francisco, CA
Key facts
| Inspection ID | 1172372 |
|---|---|
| Firm | Knox Medical Diagnostics, Inc. |
| FEI number | 3016721526 |
| Address | 345 California St Ste 600 |
| City | San Francisco |
| State | CA |
| ZIP | 94108 |
| Country | United States |
| Fiscal year | 2022 |
| Inspection end date | Jun 21, 2022 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data