FDA inspection
Organon USA Inc.: FDA inspection ending Jun 6, 2000
FDA inspection 25071 · Voluntary Action Indicated (VAI) · West Orange, NJ
Key facts
| Inspection ID | 25071 |
|---|---|
| Firm | Organon USA Inc. |
| FEI number | 2211109 |
| Address | 375 Mount Pleasant Ave |
| City | West Orange |
| State | NJ |
| ZIP | 07052-2724 |
| Fiscal year | 2000 |
| Inspection end date | Jun 6, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| 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
- 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