FDA inspection
Pfizer Inc. Groton Laboratories: FDA inspection ending Feb 4, 2004
FDA inspection 314921 · No Action Indicated (NAI) · Groton, CT
Key facts
| Inspection ID | 314921 |
|---|---|
| Firm | Pfizer Inc. Groton Laboratories |
| FEI number | 1216806 |
| Address | Eastern Point Rd, Building 274 |
| City | Groton |
| State | CT |
| ZIP | 06340 |
| Fiscal year | 2004 |
| Inspection end date | Feb 4, 2004 |
| Classification | No Action Indicated (NAI) |
| Project area | Pre-Apprvl of Animal Drugs/Food Addit |
| Product type | Drugs |
At a glance
- None Citations
- None 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