FDA inspection

Kleen Test Products Corporation: FDA inspection ending Nov 30, 2009

FDA inspection 634732 · Voluntary Action Indicated (VAI) · Port Washington, WI

Key facts

Inspection ID 634732
Firm Kleen Test Products Corporation
FEI number 3004586080
Address 1611 S Sunset Rd
City Port Washington
State WI
ZIP 53074
Country United States
Fiscal year 2010
Inspection end date Nov 30, 2009
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

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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