FDA inspection

Lonza AG: FDA inspection ending Oct 3, 2012

FDA inspection 807642 · Voluntary Action Indicated (VAI) · Visp

Key facts

Inspection ID 807642
Firm Lonza AG
FEI number 3002930340
Address Lonzastrasse 2
City Visp
Fiscal year 2013
Inspection end date Oct 3, 2012
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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