FDA inspection
3M Company: FDA inspection ending Aug 16, 2010
FDA inspection 684056 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 684056 |
|---|---|
| Firm | 3M Company |
| FEI number | 2110898 |
| Address | 3m Center 2510 Conway Ave, Bldg 275-5W-06 |
| City | Saint Paul |
| State | MN |
| ZIP | 55144 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Aug 16, 2010 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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