FDA inspection
Lixi Corporation: FDA inspection ending Oct 12, 2004
FDA inspection 348603 · Voluntary Action Indicated (VAI) · Carpentersville, IL
Key facts
| Inspection ID | 348603 |
|---|---|
| Firm | Lixi Corporation |
| FEI number | 1419514 |
| Address | 120 S Lincoln Ave |
| City | Carpentersville |
| State | IL |
| ZIP | 60110-1703 |
| Fiscal year | 2005 |
| Inspection end date | Oct 12, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Rad Cntrl & Hlth Safety Act (RCHSA) Auth |
| 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