FDA inspection

Lonza Biologics, Inc.: FDA inspection ending Jun 6, 2025

FDA inspection 1269735 · Voluntary Action Indicated (VAI) · Portsmouth, NH

Key facts

Inspection ID 1269735
Firm Lonza Biologics, Inc.
FEI number 3001451441
Address 101 International Dr
City Portsmouth
State NH
ZIP 03801-2846
Fiscal year 2025
Inspection end date Jun 6, 2025
Classification Voluntary Action Indicated (VAI)
Project area Human Cellular, Tissue, and Gene Therapies
Product type Biologics, Drugs

At a glance

  • None Citations
  • 1–9 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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