FDA inspection

Eurofins Lancaster Laboratories, Inc: FDA inspection ending May 3, 2000

FDA inspection 23557 · No Action Indicated (NAI) · Lancaster, PA

Key facts

Inspection ID 23557
Firm Eurofins Lancaster Laboratories, Inc
FEI number 2513291
Address 2425 New Holland Pike
City Lancaster
State PA
ZIP 17601-5946
Fiscal year 2000
Inspection end date May 3, 2000
Classification No Action Indicated (NAI)
Project area New Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No 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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