FDA inspection
Pfizer, Inc.: FDA inspection ending Dec 13, 2024
FDA inspection 1256477 · Voluntary Action Indicated (VAI) · Groton, CT
Key facts
| Inspection ID | 1256477 |
|---|---|
| Firm | Pfizer, Inc. |
| FEI number | 1211022 |
| Address | 445 Eastern Point Rd |
| City | Groton |
| State | CT |
| ZIP | 06340 |
| Fiscal year | 2025 |
| Inspection end date | Dec 13, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring: Human Drugs |
| Product type | Drugs |
At a glance
- 1–9 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