FDA inspection

Apex Pharmaceuticals Inc.: FDA inspection ending Apr 18, 2019

FDA inspection 1086635 · Voluntary Action Indicated (VAI) · South Plainfield, NJ

Key facts

Inspection ID 1086635
Firm Apex Pharmaceuticals Inc.
FEI number 3006719767
Address 3005 Hadley Rd Ste 8
City South Plainfield
State NJ
ZIP 07080
Country United States
Fiscal year 2019
Inspection end date Apr 18, 2019
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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