FDA inspection

Lake Forest Hospital (IRC): FDA inspection ending Apr 15, 2003

FDA inspection 260710 · Official Action Indicated (OAI) · Lake Forest, IL

Key facts

Inspection ID 260710
Firm Lake Forest Hospital (IRC)
FEI number 1420276
Address 660 N Westmoreland Rd
City Lake Forest
State IL
ZIP 60045-1659
Fiscal year 2003
Inspection end date Apr 15, 2003
Classification Official Action Indicated (OAI)
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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