FDA inspection
Irenda Corporation: FDA inspection ending Mar 11, 2004
FDA inspection 333737 · Los Angeles, CA
Key facts
| Inspection ID | 333737 |
|---|---|
| Firm | Irenda Corporation |
| FEI number | 2050154 |
| Address | 14131 Avalon Blvd |
| City | Los Angeles |
| State | CA |
| ZIP | 90061-2637 |
| Fiscal year | 2004 |
| Inspection end date | Mar 11, 2004 |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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