FDA inspection
MIE America, Inc.: FDA inspection ending Jan 8, 2018
FDA inspection 1037046 · Voluntary Action Indicated (VAI) · Elk Grove Village, IL
Key facts
| Inspection ID | 1037046 |
|---|---|
| Firm | MIE America, Inc. |
| FEI number | 3000210013 |
| Address | 420 Bennett Rd |
| City | Elk Grove Village |
| State | IL |
| ZIP | 60007 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jan 8, 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