FDA inspection
KBL GmbH: FDA inspection ending Jun 15, 2023
FDA inspection 1210373 · No Action Indicated (NAI) · Dernbach
Key facts
| Inspection ID | 1210373 |
|---|---|
| Firm | KBL GmbH |
| FEI number | 3006116732 |
| Address | Industriepark Urbacher Wald, Ringstr. 24-26 |
| City | Dernbach |
| Country | Germany |
| Fiscal year | 2023 |
| Inspection end date | Jun 15, 2023 |
| 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