FDA inspection
KBD, Inc.: FDA inspection ending Mar 12, 2004
FDA inspection 316877 · Official Action Indicated (OAI) · North Las Vegas, NV
Key facts
| Inspection ID | 316877 |
|---|---|
| Firm | KBD, Inc. |
| FEI number | 1022129 |
| Address | 4208 W Cheyenne Ave Ste 120 |
| City | North Las Vegas |
| State | NV |
| ZIP | 89032-3534 |
| Fiscal year | 2004 |
| Inspection end date | Mar 12, 2004 |
| Classification | Official Action Indicated (OAI) |
| 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