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FDA Inspection
•Charles River Laboratories Inc•October 17, 2025

Charles River Laboratories Inc – FDA Inspection, Oct 17, 2025

Record Details

This FDA Inspection record concerns Charles River Laboratories Inc, with an inspection on October 17, 2025, issued by the New Orleans District Office, covering biologics.

Company
Charles River Laboratories Inc
Inspection Date
October 17, 2025
Product Type
Biologics
Office
New Orleans District Office
People
  • Christine Harman (Investigator)
  • Shaina R. Fullwood (Issuing Officer)
View Company Profile

ID · d0b299ab-d1cb-40c7-bbe1-9709baca33b4

Inspection Facts

Inspection number
1294508
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Charles River Laboratories Inc

6
DateClassificationOfficeProject area
February 7, 2025Not classifiedNew Orleans District OfficeHuman Cellular, Tissue, and Gene Therapies
October 11, 2024Not classifiedNew Orleans District Office
November 17, 2023NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 25, 2023Not classifiedNew Orleans District Office
January 23, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Charles River Laboratories Inc
  • FDA Inspection 1260289 - 2025-02-07
  • FDA Inspection 1258366 - 2024-10-11
  • FDA Inspection 1224863 - 2023-11-17
  • FDA Inspection 1223136 - 2023-08-25
  • FDA Inspection 911880 - 2015-01-23

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