FDA inspection
NextPhase Medical Devices: FDA inspection ending Oct 16, 2000
FDA inspection 44245 · Voluntary Action Indicated (VAI) · Waldwick, NJ
Key facts
| Inspection ID | 44245 |
|---|---|
| Firm | NextPhase Medical Devices |
| FEI number | 3002882053 |
| Address | 150 Hopper Ave |
| City | Waldwick |
| State | NJ |
| ZIP | 07463-1513 |
| Fiscal year | 2001 |
| Inspection end date | Oct 16, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None 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