FDA inspection
Strub Medical GmbH & Co. KG: FDA inspection ending Sep 26, 2024
FDA inspection 1250923 · Voluntary Action Indicated (VAI) · Neuhausen Ob Eck
Key facts
| Inspection ID | 1250923 |
|---|---|
| Firm | Strub Medical GmbH & Co. KG |
| FEI number | 3000226659 |
| Address | Robert-Bosch-Str. 11 |
| City | Neuhausen Ob Eck |
| Country | Germany |
| Fiscal year | 2024 |
| Inspection end date | Sep 26, 2024 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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