FDA inspection

George Taub Products & Fusion Co., Inc.: FDA inspection ending Nov 20, 2024

FDA inspection 1255231 · Voluntary Action Indicated (VAI) · Jersey City, NJ

Key facts

Inspection ID 1255231
Firm George Taub Products & Fusion Co., Inc.
FEI number 2241860
Address 277 New York Ave
City Jersey City
State NJ
ZIP 07307
Country United States
Fiscal year 2025
Inspection end date Nov 20, 2024
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

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