FDA inspection
Orthometrix, Inc.: FDA inspection ending Mar 5, 2005
FDA inspection 368489 · Official Action Indicated (OAI) · Naples, FL
Key facts
| Inspection ID | 368489 |
|---|---|
| Firm | Orthometrix, Inc. |
| FEI number | 1000610068 |
| Address | 5621 Strand Blvd, Ste 111 |
| City | Naples |
| State | FL |
| ZIP | 34110-7301 |
| Fiscal year | 2005 |
| Inspection end date | Mar 5, 2005 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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