FDA inspection
Creganna Medical Devices: FDA inspection ending Aug 18, 2016
FDA inspection 985013 · No Action Indicated (NAI) · Galway
Key facts
| Inspection ID | 985013 |
|---|---|
| Firm | Creganna Medical Devices |
| FEI number | 3004193842 |
| Address | Parkmore House, Mweeloon |
| City | Galway |
| Country | Ireland |
| Fiscal year | 2016 |
| Inspection end date | Aug 18, 2016 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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