FDA inspection
Defibtech, LLC: FDA inspection ending Aug 27, 2015
FDA inspection 940792 · No Action Indicated (NAI) · Seymour, CT
Key facts
| Inspection ID | 940792 |
|---|---|
| Firm | Defibtech, LLC |
| FEI number | 3006403206 |
| Address | 4 Progress Ave |
| City | Seymour |
| State | CT |
| ZIP | 06483 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Aug 27, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Postmarket Assurance: 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