FDA inspection
Lombart Instrument, Inc.: FDA inspection ending Nov 21, 2012
FDA inspection 808901 · Voluntary Action Indicated (VAI) · Jacksonville, FL
Key facts
| Inspection ID | 808901 |
|---|---|
| Firm | Lombart Instrument, Inc. |
| FEI number | 1041845 |
| Address | 11825 Central Pkwy |
| City | Jacksonville |
| State | FL |
| ZIP | 32224 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Nov 21, 2012 |
| 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