FDA inspection
Skytron, LLC: FDA inspection ending Apr 6, 2015
FDA inspection 920634 · Voluntary Action Indicated (VAI) · Grand Rapids, MI
Key facts
| Inspection ID | 920634 |
|---|---|
| Firm | Skytron, LLC |
| FEI number | 1825014 |
| Address | 5085 Corporate Exchange Blvd SE |
| City | Grand Rapids |
| State | MI |
| ZIP | 49512 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Apr 6, 2015 |
| 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