FDA inspection
Hampton Research & Engineering, Inc: FDA inspection ending Sep 23, 2004
FDA inspection 348192 · Voluntary Action Indicated (VAI) · Oklahoma City, OK
Key facts
| Inspection ID | 348192 |
|---|---|
| Firm | Hampton Research & Engineering, Inc |
| FEI number | 1622033 |
| Address | 2726 N Oklahoma Ave |
| City | Oklahoma City |
| State | OK |
| ZIP | 73105-2725 |
| Fiscal year | 2004 |
| Inspection end date | Sep 23, 2004 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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