FDA inspection

Beckman Coulter, Inc.: FDA inspection ending Jun 19, 2013

FDA inspection 837631 · Voluntary Action Indicated (VAI) · Chaska, MN

Key facts

Inspection ID 837631
Firm Beckman Coulter, Inc.
FEI number 2122870
Address 1000 Lake Hazeltine Dr
City Chaska
State MN
ZIP 55318
Country United States
Fiscal year 2013
Inspection end date Jun 19, 2013
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
  • 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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