FDA inspection
UreSil LLC: FDA inspection ending Jan 10, 2003
FDA inspection 252952 · No Action Indicated (NAI) · Skokie, IL
Key facts
| Inspection ID | 252952 |
|---|---|
| Firm | UreSil LLC |
| FEI number | 1450395 |
| Address | 5418 Touhy Ave |
| City | Skokie |
| State | IL |
| ZIP | 60077-3232 |
| Fiscal year | 2003 |
| Inspection end date | Jan 10, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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