FDA inspection
WAVELIGHT GmbH: FDA inspection ending Jan 28, 2010
FDA inspection 643977 · Voluntary Action Indicated (VAI) · ERLANGEN
Key facts
| Inspection ID | 643977 |
|---|---|
| Firm | WAVELIGHT GmbH |
| FEI number | 3002483854 |
| Address | Nordostpark 100-102 |
| City | ERLANGEN |
| Country | Germany |
| Fiscal year | 2010 |
| Inspection end date | Jan 28, 2010 |
| 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