FDA inspection
Iapyx Medical: FDA inspection ending Mar 14, 2005
FDA inspection 389201 · Voluntary Action Indicated (VAI) · Poway, CA
Key facts
| Inspection ID | 389201 |
|---|---|
| Firm | Iapyx Medical |
| FEI number | 3004500043 |
| Address | 12675 Stowe Dr Ste B |
| City | Poway |
| State | CA |
| ZIP | 92064-8848 |
| Fiscal year | 2005 |
| Inspection end date | Mar 14, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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