FDA inspection

Cerner Corp: FDA inspection ending May 23, 2006

FDA inspection 428591 · No Action Indicated (NAI) · Kansas City, MO

Key facts

Inspection ID 428591
Firm Cerner Corp
FEI number 1931259
Address 2800 Rock Creek Pkwy
City Kansas City
State MO
ZIP 64117-2521
Fiscal year 2006
Inspection end date May 23, 2006
Classification No Action Indicated (NAI)
Project area Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices|Blood and Blood Products|Compliance: Med Devices|Postmarket Assurance: Med Devices
Product type Biologics, Devices

At a glance

  • None Citations
  • None 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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