FDA inspection
Intricon Corp: FDA inspection ending Jan 24, 2017
FDA inspection 1000142 · No Action Indicated (NAI) · Arden Hills, MN
Key facts
| Inspection ID | 1000142 |
|---|---|
| Firm | Intricon Corp |
| FEI number | 3003007876 |
| Address | 1260 Red Fox Rd |
| City | Arden Hills |
| State | MN |
| ZIP | 55112 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Jan 24, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Project Evaluation: 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