FDA inspection
Coloplast Manufacturing US, LLC: FDA inspection ending Jul 10, 2006
FDA inspection 433596 · No Action Indicated (NAI) · North Mankato, MN
Key facts
| Inspection ID | 433596 |
|---|---|
| Firm | Coloplast Manufacturing US, LLC |
| FEI number | 2125337 |
| Address | 1940 Commerce Dr |
| City | North Mankato |
| State | MN |
| ZIP | 56003-1700 |
| Fiscal year | 2006 |
| Inspection end date | Jul 10, 2006 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med 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