FDA inspection
Bytec Medizintechnik GmbH: FDA inspection ending Jul 11, 2024
FDA inspection 1245848 · No Action Indicated (NAI) · Eschweiler
Key facts
| Inspection ID | 1245848 |
|---|---|
| Firm | Bytec Medizintechnik GmbH |
| FEI number | 3001427085 |
| Address | Hermann-Hollerith-Str. 11 |
| City | Eschweiler |
| Country | Germany |
| Fiscal year | 2024 |
| Inspection end date | Jul 11, 2024 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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