FDA inspection
HeartSine Technologies Ltd: FDA inspection ending Feb 12, 2015
FDA inspection 918076 · No Action Indicated (NAI) · Belfast
Key facts
| Inspection ID | 918076 |
|---|---|
| Firm | HeartSine Technologies Ltd |
| FEI number | 3004123209 |
| Address | Canberra House, Canberra House |
| City | Belfast |
| Country | United Kingdom |
| Fiscal year | 2015 |
| Inspection end date | Feb 12, 2015 |
| 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