FDA inspection
3M Company: FDA inspection ending Apr 20, 2012
FDA inspection 778370 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 778370 |
|---|---|
| Firm | 3M Company |
| FEI number | 2126770 |
| Address | 2510 Conway Ave E |
| City | Saint Paul |
| State | MN |
| ZIP | 55144 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Apr 20, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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