FDA inspection
Remel Inc: FDA inspection ending Apr 10, 2008
FDA inspection 520376 · Voluntary Action Indicated (VAI) · Lenexa, KS
Key facts
| Inspection ID | 520376 |
|---|---|
| Firm | Remel Inc |
| FEI number | 1924669 |
| Address | 12076 Santa Fe Trail Dr |
| City | Lenexa |
| State | KS |
| ZIP | 66215-3519 |
| Fiscal year | 2008 |
| Inspection end date | Apr 10, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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