FDA inspection
Skytron, Div. The KMW Group, Inc: FDA inspection ending Aug 15, 2007
FDA inspection 488086 · Voluntary Action Indicated (VAI) · Grand Rapids, MI
Key facts
| Inspection ID | 488086 |
|---|---|
| Firm | Skytron, Div. The KMW Group, Inc |
| FEI number | 1825014 |
| Address | 5085 Corporate Exchange Blvd SE |
| City | Grand Rapids |
| State | MI |
| ZIP | 49512-5515 |
| Fiscal year | 2007 |
| Inspection end date | Aug 15, 2007 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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