FDA inspection
Tulip Medical Products: FDA inspection ending Jan 26, 2010
FDA inspection 640576 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 640576 |
|---|---|
| Firm | Tulip Medical Products |
| FEI number | 1000518699 |
| Address | 4360 Morena Blvd Ste 100 |
| City | San Diego |
| State | CA |
| ZIP | 92117 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Jan 26, 2010 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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