FDA inspection
Merz North America Inc.: FDA inspection ending Jul 13, 2017
FDA inspection 1029900 · No Action Indicated (NAI) · Sturtevant, WI
Key facts
| Inspection ID | 1029900 |
|---|---|
| Firm | Merz North America Inc. |
| FEI number | 3013840437 |
| Address | 13900 Grandview Pkwy W |
| City | Sturtevant |
| State | WI |
| ZIP | 53177-1275 |
| Fiscal year | 2017 |
| Inspection end date | Jul 13, 2017 |
| 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
- 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