FDA inspection
NextPhase Medical Devices LLC: FDA inspection ending Mar 22, 2006
FDA inspection 421101 · Voluntary Action Indicated (VAI) · Rochester, NH
Key facts
| Inspection ID | 421101 |
|---|---|
| Firm | NextPhase Medical Devices LLC |
| FEI number | 3001237338 |
| Address | 88 Airport Dr |
| City | Rochester |
| State | NH |
| ZIP | 03867-1706 |
| Fiscal year | 2006 |
| Inspection end date | Mar 22, 2006 |
| 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