FDA inspection
Dupont Pharmaceuticals Company: FDA inspection ending May 23, 2000
FDA inspection 23712 · Voluntary Action Indicated (VAI) · Wilmington, DE
Key facts
| Inspection ID | 23712 |
|---|---|
| Firm | Dupont Pharmaceuticals Company |
| FEI number | 1000121571 |
| Address | 974 Centre Rd |
| City | Wilmington |
| State | DE |
| ZIP | 19805-1269 |
| Fiscal year | 2000 |
| Inspection end date | May 23, 2000 |
| 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
- 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