FDA inspection
Pulse Biomedical Inc: FDA inspection ending Nov 6, 2017
FDA inspection 1030842 · Voluntary Action Indicated (VAI) · King Of Prussia, PA
Key facts
| Inspection ID | 1030842 |
|---|---|
| Firm | Pulse Biomedical Inc |
| FEI number | 1000121413 |
| Address | 112 Ivy Ln |
| City | King Of Prussia |
| State | PA |
| ZIP | 19406 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Nov 6, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| 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
- 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