FDA inspection
Grand Medical: FDA inspection ending Nov 20, 2009
FDA inspection 631022 · Voluntary Action Indicated (VAI) · Kansas City, MO
Key facts
| Inspection ID | 631022 |
|---|---|
| Firm | Grand Medical |
| FEI number | 3004873266 |
| Address | 8206 NW High Point Dr |
| City | Kansas City |
| State | MO |
| ZIP | 64152 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Nov 20, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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