FDA inspection
3M Company: FDA inspection ending Apr 13, 2011
FDA inspection 720685 · Voluntary Action Indicated (VAI) · Cordova, IL
Key facts
| Inspection ID | 720685 |
|---|---|
| Firm | 3M Company |
| FEI number | 1484185 |
| Address | 22614 Route 84 N Bldg 3and23 |
| City | Cordova |
| State | IL |
| ZIP | 61242 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Apr 13, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
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
- 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