FDA inspection
AtriCure: FDA inspection ending Sep 30, 2016
FDA inspection 995786 · No Action Indicated (NAI) · Minnetonka, MN
Key facts
| Inspection ID | 995786 |
|---|---|
| Firm | AtriCure |
| FEI number | 3011788769 |
| Address | 130 Cheshire Ln Ste 250 |
| City | Minnetonka |
| State | MN |
| ZIP | 55305-1027 |
| Fiscal year | 2016 |
| Inspection end date | Sep 30, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes 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