FDA inspection
STERIS MEXICO, S. de R.L. de C.V.: FDA inspection ending Jul 19, 2019
FDA inspection 1142941 · Voluntary Action Indicated (VAI) · Guadalupe
Key facts
| Inspection ID | 1142941 |
|---|---|
| Firm | STERIS MEXICO, S. de R.L. de C.V. |
| FEI number | 3005899764 |
| Address | Avenida Avante 790, Zona Industrial Parque Industrial Guadalupe, Guadalupe |
| City | Guadalupe |
| Fiscal year | 2019 |
| Inspection end date | Jul 19, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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