FDA inspection
Ft Wayne Metal Resch Prod Corp: FDA inspection ending May 10, 2024
FDA inspection 1230521 · Voluntary Action Indicated (VAI) · Fort Wayne, IN
Key facts
| Inspection ID | 1230521 |
|---|---|
| Firm | Ft Wayne Metal Resch Prod Corp |
| FEI number | 1824313 |
| Address | 9609 Ardmore Ave |
| City | Fort Wayne |
| State | IN |
| ZIP | 46809 |
| Country | United States |
| Fiscal year | 2024 |
| Inspection end date | May 10, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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