FDA inspection
KBD, Inc.: FDA inspection ending Dec 23, 2016
FDA inspection 998372 · Voluntary Action Indicated (VAI) · North Las Vegas, NV
Key facts
| Inspection ID | 998372 |
|---|---|
| Firm | KBD, Inc. |
| FEI number | 1022129 |
| Address | 7240 W Azure Dr Ste 160 |
| City | North Las Vegas |
| State | NV |
| ZIP | 89032 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Dec 23, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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