FDA inspection
Diapulse Corporation of America: FDA inspection ending Jun 10, 2009
FDA inspection 587890 · Voluntary Action Indicated (VAI) · Great Neck, NY
Key facts
| Inspection ID | 587890 |
|---|---|
| Firm | Diapulse Corporation of America |
| FEI number | 2410367 |
| Address | 475 Northern Blvd Ste 33 |
| City | Great Neck |
| State | NY |
| ZIP | 11021 |
| Country | United States |
| Fiscal year | 2009 |
| Inspection end date | Jun 10, 2009 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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