FDA inspection
LimFlow, Inc.: FDA inspection ending May 15, 2023
FDA inspection 1205879 · Voluntary Action Indicated (VAI) · Irvine, CA
Key facts
| Inspection ID | 1205879 |
|---|---|
| Firm | LimFlow, Inc. |
| FEI number | 3023527320 |
| Address | 3031 Tisch Way Ste 110 |
| City | Irvine |
| State | CA |
| ZIP | 92618 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | May 15, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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