FDA inspection
Simmler Inc: FDA inspection ending May 10, 2002
FDA inspection 232212 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 232212 |
|---|---|
| Firm | Simmler Inc |
| FEI number | 1950226 |
| Address | 2115 59th St |
| City | Saint Louis |
| State | MO |
| ZIP | 63110-2807 |
| Fiscal year | 2002 |
| Inspection end date | May 10, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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