FDA inspection
Pulmonx, Corp.: FDA inspection ending Feb 28, 2008
FDA inspection 509941 · No Action Indicated (NAI) · Redwood City, CA
Key facts
| Inspection ID | 509941 |
|---|---|
| Firm | Pulmonx, Corp. |
| FEI number | 3007797756 |
| Address | 700 Chesapeake Dr |
| City | Redwood City |
| State | CA |
| ZIP | 94063-4731 |
| Fiscal year | 2008 |
| Inspection end date | Feb 28, 2008 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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