FDA inspection
Medtox Laboratories, Inc.: FDA inspection ending Aug 21, 2009
FDA inspection 609775 · Voluntary Action Indicated (VAI) · Saint Paul, MN
Key facts
| Inspection ID | 609775 |
|---|---|
| Firm | Medtox Laboratories, Inc. |
| FEI number | 3001239310 |
| Address | 402 County Road D W |
| City | Saint Paul |
| State | MN |
| ZIP | 55112-3522 |
| Fiscal year | 2009 |
| Inspection end date | Aug 21, 2009 |
| 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
- Yes Establishment inspection report (EIR) exists
- 1–9 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