FDA inspection
Pulmonx, Corp.: FDA inspection ending Dec 11, 2007
FDA inspection 502220 · Official Action Indicated (OAI) · Redwood City, CA
Key facts
| Inspection ID | 502220 |
|---|---|
| Firm | Pulmonx, Corp. |
| FEI number | 3007797756 |
| Address | 700 Chesapeake Dr |
| City | Redwood City |
| State | CA |
| ZIP | 94063-4731 |
| Fiscal year | 2008 |
| Inspection end date | Dec 11, 2007 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med 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