FDA inspection

Lonza Biologics, Inc.: FDA inspection ending Mar 7, 2024

FDA inspection 1232144 · Voluntary Action Indicated (VAI) · Portsmouth, NH

Key facts

Inspection ID 1232144
Firm Lonza Biologics, Inc.
FEI number 3001451441
Address 101 International Dr
City Portsmouth
State NH
ZIP 03801
Country United States
Fiscal year 2024
Inspection end date Mar 7, 2024
Classification Voluntary Action Indicated (VAI)
Project area Vaccines and Allergenic Products
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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