FDA inspection
ILMO PRODUCTS COMPANY: FDA inspection ending Jul 31, 2012
FDA inspection 792606 · No Action Indicated (NAI) · Mount Vernon, IL
Key facts
| Inspection ID | 792606 |
|---|---|
| Firm | ILMO PRODUCTS COMPANY |
| FEI number | 3003574148 |
| Address | 2422 Benton Rd |
| City | Mount Vernon |
| State | IL |
| ZIP | 62864 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Jul 31, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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