FDA inspection
Harmac Medical Products, Ltd.: FDA inspection ending Mar 21, 2008
FDA inspection 513876 · Voluntary Action Indicated (VAI) · Castlerea
Key facts
| Inspection ID | 513876 |
|---|---|
| Firm | Harmac Medical Products, Ltd. |
| FEI number | 3002468842 |
| Address | Ida Business Park |
| City | Castlerea |
| Fiscal year | 2008 |
| Inspection end date | Mar 21, 2008 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 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