FDA inspection
STERIS Corporation: FDA inspection ending Jul 16, 2009
FDA inspection 599535 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 599535 |
|---|---|
| Firm | STERIS Corporation |
| FEI number | 1937531 |
| Address | 7501 Page Ave |
| City | Saint Louis |
| State | MO |
| ZIP | 63133 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jul 16, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None 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