FDA inspection
WAVELIGHT GmbH: FDA inspection ending Jul 21, 2011
FDA inspection 739987 · No Action Indicated (NAI) · ERLANGEN
Key facts
| Inspection ID | 739987 |
|---|---|
| Firm | WAVELIGHT GmbH |
| FEI number | 3002483854 |
| Address | Nordostpark 100-102 |
| City | ERLANGEN |
| Country | Germany |
| Fiscal year | 2011 |
| Inspection end date | Jul 21, 2011 |
| 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