FDA inspection

Charles River Laboratories Inc.: FDA inspection ending Jun 2, 2006

FDA inspection 428557 · No Action Indicated (NAI) · Frederick, MD

Key facts

Inspection ID 428557
Firm Charles River Laboratories Inc.
FEI number 1121382
Address 15 Wormans Mill Ct Ste I
City Frederick
State MD
ZIP 21701-3019
Fiscal year 2006
Inspection end date Jun 2, 2006
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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