FDA inspection
Elixir Corporation: FDA inspection ending Jan 10, 2018
FDA inspection 1039236 · No Action Indicated (NAI) · Suwanee, GA
Key facts
| Inspection ID | 1039236 |
|---|---|
| Firm | Elixir Corporation |
| FEI number | 3008513006 |
| Address | 305 Shawnee Dr N Ste 250 |
| City | Suwanee |
| State | GA |
| ZIP | 30024 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jan 10, 2018 |
| 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