FDA inspection
Smith & Nephew Inc.: FDA inspection ending Mar 26, 2015
FDA inspection 920985 · Official Action Indicated (OAI) · Andover, MA
Key facts
| Inspection ID | 920985 |
|---|---|
| Firm | Smith & Nephew Inc. |
| FEI number | 3003604053 |
| Address | 150 Minuteman Rd |
| City | Andover |
| State | MA |
| ZIP | 01810 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Mar 26, 2015 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 457814 |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- Yes 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