FDA inspection
Organon USA Inc.: FDA inspection ending Mar 25, 2002
FDA inspection 205465 · Voluntary Action Indicated (VAI) · West Orange, NJ
Key facts
| Inspection ID | 205465 |
|---|---|
| Firm | Organon USA Inc. |
| FEI number | 2211109 |
| Address | 375 Mount Pleasant Ave |
| City | West Orange |
| State | NJ |
| ZIP | 07052-2724 |
| Fiscal year | 2002 |
| Inspection end date | Mar 25, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bio-Research Monit: Human Drugs |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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