FDA inspection

Lonza AG: FDA inspection ending May 21, 2019

FDA inspection 1091799 · Voluntary Action Indicated (VAI) · Visp

Key facts

Inspection ID 1091799
Firm Lonza AG
FEI number 3002930340
Address Lonzastrasse 2
City Visp
Fiscal year 2019
Inspection end date May 21, 2019
Classification Voluntary Action Indicated (VAI)
Project area New Drug Evaluation
Product type 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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