FDA inspection

Entrogen, Inc: FDA inspection ending May 14, 2026

FDA inspection 1323306 · No Action Indicated (NAI) · Woodland Hills, CA

Key facts

Inspection ID 1323306
Firm Entrogen, Inc
FEI number 3010791816
Address 20950 Warner Center Ln Ste B
City Woodland Hills
State CA
ZIP 91367
Country United States
Fiscal year 2026
Inspection end date May 14, 2026
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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