FDA inspection
Coloplast Manufacturing US, LLC: FDA inspection ending Jan 20, 2023
FDA inspection 1196697 · No Action Indicated (NAI) · Minneapolis, MN
Key facts
| Inspection ID | 1196697 |
|---|---|
| Firm | Coloplast Manufacturing US, LLC |
| FEI number | 2125050 |
| Address | 1601 W River Rd |
| City | Minneapolis |
| State | MN |
| ZIP | 55411 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Jan 20, 2023 |
| 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