FDA inspection

DermaRite Industries, LLC: FDA inspection ending Apr 8, 2025

FDA inspection 1250450 · Official Action Indicated (OAI) · North Bergen, NJ

Key facts

Inspection ID 1250450
Firm DermaRite Industries, LLC
FEI number 1000526900
Address 7777 W Side Ave
City North Bergen
State NJ
ZIP 07047
Country United States
Fiscal year 2025
Inspection end date Apr 8, 2025
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs
Warning letter 710997

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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