FDA inspection
Nutek Orthopaedics, Inc.: FDA inspection ending Jan 4, 2018
FDA inspection 1036749 · Voluntary Action Indicated (VAI) · Fort Lauderdale, FL
Key facts
| Inspection ID | 1036749 |
|---|---|
| Firm | Nutek Orthopaedics, Inc. |
| FEI number | 3005893246 |
| Address | 641 SW 3rd Ave |
| City | Fort Lauderdale |
| State | FL |
| ZIP | 33315 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jan 4, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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