FDA inspection
Stoelting Co./Div. Of Autogeni: FDA inspection ending Apr 17, 2002
FDA inspection 212521 · Voluntary Action Indicated (VAI) · Wood Dale, IL
Key facts
| Inspection ID | 212521 |
|---|---|
| Firm | Stoelting Co./Div. Of Autogeni |
| FEI number | 1417837 |
| Address | 620 Wheat Ln |
| City | Wood Dale |
| State | IL |
| ZIP | 60191-1102 |
| Fiscal year | 2002 |
| Inspection end date | Apr 17, 2002 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 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