FDA inspection
Ad-Tech Medical Instrument Corporation: FDA inspection ending Nov 26, 2012
FDA inspection 808283 · Voluntary Action Indicated (VAI) · Oak Creek, WI
Key facts
| Inspection ID | 808283 |
|---|---|
| Firm | Ad-Tech Medical Instrument Corporation |
| FEI number | 2183456 |
| Address | 400 W Oakview Pkwy |
| City | Oak Creek |
| State | WI |
| ZIP | 53154 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Nov 26, 2012 |
| 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
- 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