FDA inspection
Smith & Nephew, Inc.: FDA inspection ending Mar 20, 2003
FDA inspection 267432 · No Action Indicated (NAI) · Saint Petersburg, FL
Key facts
| Inspection ID | 267432 |
|---|---|
| Firm | Smith & Nephew, Inc. |
| FEI number | 3006760724 |
| Address | 970 Lake Carillon Dr Ste 110 |
| City | Saint Petersburg |
| State | FL |
| ZIP | 33716-1130 |
| Fiscal year | 2003 |
| Inspection end date | Mar 20, 2003 |
| 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