FDA inspection
Pfizer Inc. Groton Laboratories: FDA inspection ending Sep 1, 2005
FDA inspection 398933 · Voluntary Action Indicated (VAI) · Groton, CT
Key facts
| Inspection ID | 398933 |
|---|---|
| Firm | Pfizer Inc. Groton Laboratories |
| FEI number | 1216806 |
| Address | Eastern Point Rd, Building 274 |
| City | Groton |
| State | CT |
| ZIP | 06340 |
| Fiscal year | 2005 |
| Inspection end date | Sep 1, 2005 |
| 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
- 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