FDA inspection

St Joseph Mercy Health System IRB: FDA inspection ending Dec 2, 2002

FDA inspection 252045 · No Action Indicated (NAI) · Ypsilanti, MI

Key facts

Inspection ID 252045
Firm St Joseph Mercy Health System IRB
FEI number 1824719
Address 5333 McAuley Dr Rm 6017
City Ypsilanti
State MI
ZIP 48197-1005
Fiscal year 2003
Inspection end date Dec 2, 2002
Classification No Action Indicated (NAI)
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
  • 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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