FDA inspection
Merz North America, Inc.: FDA inspection ending Apr 19, 2013
FDA inspection 828392 · No Action Indicated (NAI) · Sturtevant, WI
Key facts
| Inspection ID | 828392 |
|---|---|
| Firm | Merz North America, Inc. |
| FEI number | 3013840437 |
| Address | 13900 Grandview Pkwy W |
| City | Sturtevant |
| State | WI |
| ZIP | 53177 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Apr 19, 2013 |
| Classification | No Action Indicated (NAI) |
| Project area | Project Evaluation: 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
- 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