FDA inspection
Michigan Instruments, Inc.: FDA inspection ending Dec 16, 2011
FDA inspection 759502 · Voluntary Action Indicated (VAI) · Grand Rapids, MI
Key facts
| Inspection ID | 759502 |
|---|---|
| Firm | Michigan Instruments, Inc. |
| FEI number | 1821850 |
| Address | 4717 Talon Ct SE |
| City | Grand Rapids |
| State | MI |
| ZIP | 49512 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Dec 16, 2011 |
| 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
- 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