FDA inspection
3M Company IRB: FDA inspection ending Oct 10, 2012
FDA inspection 803442 · Voluntary Action Indicated (VAI) · Saint Paul, MN
Key facts
| Inspection ID | 803442 |
|---|---|
| Firm | 3M Company IRB |
| FEI number | 3009666037 |
| Address | 3M Center Bldg 220-6E-03 |
| City | Saint Paul |
| State | MN |
| ZIP | 55144 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Oct 10, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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
- 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