FDA inspection
Elekta, Inc.: FDA inspection ending Dec 13, 2019
FDA inspection 1123129 · No Action Indicated (NAI) · Atlanta, GA
Key facts
| Inspection ID | 1123129 |
|---|---|
| Firm | Elekta, Inc. |
| FEI number | 1037831 |
| Address | 400 Perimeter Center Ter NE Ste 50 |
| City | Atlanta |
| State | GA |
| ZIP | 30346 |
| Country | United States |
| Fiscal year | 2020 |
| Inspection end date | Dec 13, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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