FDA inspection
Elekta Instrument AB: FDA inspection ending Nov 15, 2000
FDA inspection 55569 · No Action Indicated (NAI) · Stockholm
Key facts
| Inspection ID | 55569 |
|---|---|
| Firm | Elekta Instrument AB |
| FEI number | 3002806883 |
| Address | Kungstensgatan 18 |
| City | Stockholm |
| Fiscal year | 2001 |
| Inspection end date | Nov 15, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: 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