FDA inspection
Urologix LLC: FDA inspection ending Aug 17, 2007
FDA inspection 487669 · Voluntary Action Indicated (VAI) · Plymouth, MN
Key facts
| Inspection ID | 487669 |
|---|---|
| Firm | Urologix LLC |
| FEI number | 3000718675 |
| Address | 13355 10th Ave N Ste 110 |
| City | Plymouth |
| State | MN |
| ZIP | 55441-5554 |
| Fiscal year | 2007 |
| Inspection end date | Aug 17, 2007 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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