FDA inspection
Vektor Medical, Inc.: FDA inspection ending May 12, 2026
FDA inspection 1320182 · No Action Indicated (NAI) · San Diego, CA
Key facts
| Inspection ID | 1320182 |
|---|---|
| Firm | Vektor Medical, Inc. |
| FEI number | 3021016555 |
| Address | 9255 Towne Centre Dr Ste 840 |
| City | San Diego |
| State | CA |
| ZIP | 92121 |
| Country | United States |
| Fiscal year | 2026 |
| Inspection end date | May 12, 2026 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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