FDA inspection
Zenflow, Inc.: FDA inspection ending Oct 30, 2025
FDA inspection 1290048 · Voluntary Action Indicated (VAI) · South San Francisco, CA
Key facts
| Inspection ID | 1290048 |
|---|---|
| Firm | Zenflow, Inc. |
| FEI number | 3014211785 |
| Address | 395 Oyster Point Blvd Ste 501 |
| City | South San Francisco |
| State | CA |
| ZIP | 94080-1933 |
| Fiscal year | 2026 |
| Inspection end date | Oct 30, 2025 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Medical 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