FDA inspection
Wyeth Pharmaceutical Division of Wyeth Holdings LLC: FDA inspection ending Oct 24, 2012
FDA inspection 804865 · Voluntary Action Indicated (VAI) · Pearl River, NY
Key facts
| Inspection ID | 804865 |
|---|---|
| Firm | Wyeth Pharmaceutical Division of Wyeth Holdings LLC |
| FEI number | 2410662 |
| Address | 401 N Middletown Rd |
| City | Pearl River |
| State | NY |
| ZIP | 10965 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Oct 24, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Vaccines and Allergenic Products |
| Product type | Biologics |
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