FDA inspection
Gentian AS: FDA inspection ending Jun 21, 2012
FDA inspection 791023 · No Action Indicated (NAI) · Moss
Key facts
| Inspection ID | 791023 |
|---|---|
| Firm | Gentian AS |
| FEI number | 3006801241 |
| Address | Bjornasveien 5 |
| City | Moss |
| Country | Norway |
| Fiscal year | 2012 |
| Inspection end date | Jun 21, 2012 |
| Classification | No Action Indicated (NAI) |
| 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