FDA inspection
KCI USA, Inc.: FDA inspection ending Dec 9, 2005
FDA inspection 405717 · Voluntary Action Indicated (VAI) · San Antonio, TX
Key facts
| Inspection ID | 405717 |
|---|---|
| Firm | KCI USA, Inc. |
| FEI number | 3005178245 |
| Address | 6203 Farinon Dr |
| City | San Antonio |
| State | TX |
| ZIP | 78249 |
| Fiscal year | 2006 |
| Inspection end date | Dec 9, 2005 |
| 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
- 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