FDA inspection

Fenwal Inc: FDA inspection ending Mar 20, 2009

FDA inspection 571368 · Voluntary Action Indicated (VAI) · Lake Zurich, IL

Key facts

Inspection ID 571368
Firm Fenwal Inc
FEI number 3004548776
Address 3 Corporate Dr Ste 300
City Lake Zurich
State IL
ZIP 60047
Country United States
Fiscal year 2009
Inspection end date Mar 20, 2009
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No 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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