FDA inspection
Hampton Medical Devices, LLC: FDA inspection ending Dec 19, 2005
FDA inspection 406782 · No Action Indicated (NAI) · Festus, MO
Key facts
| Inspection ID | 406782 |
|---|---|
| Firm | Hampton Medical Devices, LLC |
| FEI number | 1937445 |
| Address | 6 Meadow Rdg |
| City | Festus |
| State | MO |
| ZIP | 63028-3076 |
| Fiscal year | 2006 |
| Inspection end date | Dec 19, 2005 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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
- 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