FDA inspection
Meridian Medical Technologies, Inc. dba Meridian Medical Technologies, Inc. a Pfizer Company: FDA inspection ending Jan 26, 2004
FDA inspection 311693 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 311693 |
|---|---|
| Firm | Meridian Medical Technologies, Inc. dba Meridian Medical Technologies, Inc. a Pfizer Company |
| FEI number | 1950222 |
| Address | 1945 Craig Rd |
| City | Saint Louis |
| State | MO |
| ZIP | 63146-4105 |
| Fiscal year | 2004 |
| Inspection end date | Jan 26, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| 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