FDA inspection
iRhythm Technologies Inc: FDA inspection ending Feb 28, 2013
FDA inspection 820317 · No Action Indicated (NAI) · San Francisco, CA
Key facts
| Inspection ID | 820317 |
|---|---|
| Firm | iRhythm Technologies Inc |
| FEI number | 3007208829 |
| Address | 699 8th St Ste 600 |
| City | San Francisco |
| State | CA |
| ZIP | 94103 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Feb 28, 2013 |
| 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