FDA inspection
Richard Wolf Medical Instruments Corp.: FDA inspection ending Oct 10, 2014
FDA inspection 900890 · Voluntary Action Indicated (VAI) · Vernon Hills, IL
Key facts
| Inspection ID | 900890 |
|---|---|
| Firm | Richard Wolf Medical Instruments Corp. |
| FEI number | 1418479 |
| Address | 353 Corporate Woods Pkwy |
| City | Vernon Hills |
| State | IL |
| ZIP | 60061 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Oct 10, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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
- 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