FDA inspection

Swedish Covenant Hospital IRB: FDA inspection ending Dec 18, 2003

FDA inspection 304948 · Voluntary Action Indicated (VAI) · Chicago, IL

Key facts

Inspection ID 304948
Firm Swedish Covenant Hospital IRB
FEI number 1473008
Address 5145 N California Ave
City Chicago
State IL
ZIP 60625-3661
Fiscal year 2004
Inspection end date Dec 18, 2003
Classification Voluntary Action Indicated (VAI)
Project area Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Bio-Research Monit: Human Drugs|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices|Human Cellular, Tissue and Gene Therapies|Product Evaluation: Med Devices
Product type Biologics, Devices, Drugs

At a glance

  • None 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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