FDA inspection
FluoroMed Products, L.P.: FDA inspection ending Dec 14, 2000
FDA inspection 55966 · No Action Indicated (NAI) · Round Rock, TX
Key facts
| Inspection ID | 55966 |
|---|---|
| Firm | FluoroMed Products, L.P. |
| FEI number | 3001237276 |
| Address | 2350 Double Creek Dr |
| City | Round Rock |
| State | TX |
| ZIP | 78664-3801 |
| Fiscal year | 2001 |
| Inspection end date | Dec 14, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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