FDA inspection
3M Company - Health Care Business: FDA inspection ending May 26, 2016
FDA inspection 980220 · No Action Indicated (NAI) · Saint Paul, MN
Key facts
| Inspection ID | 980220 |
|---|---|
| Firm | 3M Company - Health Care Business |
| FEI number | 2110898 |
| Address | 3m Center 2510 Conway Ave, Bldg 275-5W-06 |
| City | Saint Paul |
| State | MN |
| ZIP | 55144-0001 |
| Fiscal year | 2016 |
| Inspection end date | May 26, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes 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