FDA inspection

Eurofins BioPharma Product Testing ENCO, LLC: FDA inspection ending Aug 1, 2025

FDA inspection 1279054 · No Action Indicated (NAI) · Cary, NC

Key facts

Inspection ID 1279054
Firm Eurofins BioPharma Product Testing ENCO, LLC
FEI number 3009827154
Address 102 Woodwinds Industrial Ct
City Cary
State NC
ZIP 27511
Country United States
Fiscal year 2025
Inspection end date Aug 1, 2025
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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