FDA inspection
Diatron US Inc.: FDA inspection ending Sep 6, 2017
FDA inspection 1029220 · No Action Indicated (NAI) · Medley, FL
Key facts
| Inspection ID | 1029220 |
|---|---|
| Firm | Diatron US Inc. |
| FEI number | 3008425728 |
| Address | 12601 Nw 115th Ave ste A113 |
| City | Medley |
| State | FL |
| ZIP | 33178 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Sep 6, 2017 |
| 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