FDA inspection
Walsh Medical Devices Inc.: FDA inspection ending May 25, 2018
FDA inspection 1078070 · No Action Indicated (NAI) · Oakville
Key facts
| Inspection ID | 1078070 |
|---|---|
| Firm | Walsh Medical Devices Inc. |
| FEI number | 3002808473 |
| Address | 1200 South Service Rd W Unit 3 |
| City | Oakville |
| Fiscal year | 2018 |
| Inspection end date | May 25, 2018 |
| 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