FDA inspection
Amo Groningen BV: FDA inspection ending Jun 26, 2008
FDA inspection 527755 · Groningen
Key facts
| Inspection ID | 527755 |
|---|---|
| Firm | Amo Groningen BV |
| FEI number | 3004651700 |
| Address | Van Swietenlaan 5 |
| City | Groningen |
| Fiscal year | 2008 |
| Inspection end date | Jun 26, 2008 |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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