FDA inspection

Gentech, LLC.: FDA inspection ending Mar 3, 2000

FDA inspection 14674 · Voluntary Action Indicated (VAI) · Edison, NJ

Key facts

Inspection ID 14674
Firm Gentech, LLC.
FEI number 3001633332
Address 52 Bartha Ave
City Edison
State NJ
ZIP 08817-2418
Fiscal year 2000
Inspection end date Mar 3, 2000
Classification Voluntary Action Indicated (VAI)
Project area Unapproved and Misbranded Drugs
Product type Drugs

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

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