FDA inspection
LDR Spine USA, Inc.: FDA inspection ending Apr 21, 2011
FDA inspection 722030 · Voluntary Action Indicated (VAI) · Austin, TX
Key facts
| Inspection ID | 722030 |
|---|---|
| Firm | LDR Spine USA, Inc. |
| FEI number | 3004903783 |
| Address | 13785 Research Blvd Ste 200 |
| City | Austin |
| State | TX |
| ZIP | 78750 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Apr 21, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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