FDA inspection

Methodist Health System IRB: FDA inspection ending Oct 17, 2008

FDA inspection 545629 · No Action Indicated (NAI) · Dallas, TX

Key facts

Inspection ID 545629
Firm Methodist Health System IRB
FEI number 1629034
Address 1441 N Beckley Ave
City Dallas
State TX
ZIP 75203-1201
Fiscal year 2009
Inspection end date Oct 17, 2008
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Bioresearch Monitoring|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood 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Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices|Blood & Blood Products|Product Evaluation: Med Devices
Product type Biologics, Devices, Drugs

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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