FDA inspection
George Taub Products & Fusion Co., Inc.: FDA inspection ending Mar 31, 2006
FDA inspection 420230 · Voluntary Action Indicated (VAI) · Jersey City, NJ
Key facts
| Inspection ID | 420230 |
|---|---|
| Firm | George Taub Products & Fusion Co., Inc. |
| FEI number | 2241860 |
| Address | 277 New York Ave |
| City | Jersey City |
| State | NJ |
| ZIP | 07307-1501 |
| Fiscal year | 2006 |
| Inspection end date | Mar 31, 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