FDA inspection

Eurofins Lancaster Laboratories, LLC: FDA inspection ending Sep 23, 2025

FDA inspection 1284580 · No Action Indicated (NAI) · Lancaster, PA

Key facts

Inspection ID 1284580
Firm Eurofins Lancaster Laboratories, LLC
FEI number 2513291
Address 2425 New Holland Pike
City Lancaster
State PA
ZIP 17601
Country United States
Fiscal year 2025
Inspection end date Sep 23, 2025
Classification No Action Indicated (NAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics

At a glance

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