FDA inspection
ELEKTA INC.: FDA inspection ending Jul 14, 2000
FDA inspection 39296 · Voluntary Action Indicated (VAI) · Baltimore, MD
Key facts
| Inspection ID | 39296 |
|---|---|
| Firm | ELEKTA INC. |
| FEI number | 1121753 |
| Address | 7 Saint Paul St, Suite 1660 |
| City | Baltimore |
| State | MD |
| ZIP | 21202-1626 |
| Fiscal year | 2000 |
| Inspection end date | Jul 14, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None 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