FDA inspection

Lonza Biologics Plc: FDA inspection ending Sep 24, 2012

FDA inspection 802119 · Voluntary Action Indicated (VAI) · Wokingham

Key facts

Inspection ID 802119
Firm Lonza Biologics Plc
FEI number 3007518488
Address Unit 515, Eskdale Road
City Wokingham
Country United Kingdom
Fiscal year 2012
Inspection end date Sep 24, 2012
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 1–9 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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