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FDA Inspection
•Charles River Laboratories, Inc. DBA Charles River, Endosafe•March 27, 2026

Charles River Laboratories, Inc. DBA Charles River, Endosafe – FDA Inspection, Mar 27, 2026

Record Details

This FDA Inspection record concerns Charles River Laboratories, Inc. DBA Charles River, Endosafe, with an inspection on March 27, 2026, issued by the Atlanta District Office, covering human drugs.

Company
Charles River Laboratories, Inc. DBA Charles River, Endosafe
Inspection Date
March 27, 2026
Product Type
Human Drugs
Office
Atlanta District Office
People
  • Jennifer Lalama (FDA Associated Person)
  • Michael Z. Weigman (Investigator)
View Company Profile

ID · 201b3077-fdd7-494c-b29c-96b3e1fef2f6

Inspection Facts

Inspection number
1309514
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 211.22(d)Procedures not in writing, fully followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Charles River Laboratories, Inc. DBA Charles River, Endosafe

6
DateClassificationOfficeProject area
August 20, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 17, 2019VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 13, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 24, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 15, 2013VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Charles River Laboratories, Inc. DBA Charles River, Endosafe
  • FDA Inspection 1120385 - 2019-08-20
  • FDA Inspection 1091172 - 2019-05-17
  • FDA Inspection 961187 - 2016-01-13
  • FDA Inspection 876149 - 2014-04-24
  • FDA Inspection 819221 - 2013-01-15

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