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FDA Inspection
•CorePharma, LLC•August 28, 2025

CorePharma, LLC – FDA Inspection, Aug 28, 2025

Record Details

This FDA Inspection record concerns CorePharma, LLC, with an inspection on August 28, 2025, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
CorePharma, LLC
Inspection Date
August 28, 2025
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Betsy C. Galliher (Issuing Officer)
View Company Profile

ID · a79456c1-10bd-4a42-b391-e30e7bd8084c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1280399
FDA center
Human Drugs
Project area
Bioresearch Monitoring

Other FDA inspections of CorePharma, LLC

13
DateClassificationOfficeProject area
September 12, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 29, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 13, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 11, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 24, 2015NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
View all 13 other inspections on the company page
Other documents for CorePharma, LLC
  • FDA Inspection 1240419 - 2024-09-12
  • FDA Inspection 1087306 - 2019-03-29
  • FDA Inspection 1029942 - 2017-10-13
  • FDA Inspection 980585 - 2016-08-11
  • FDA Inspection 915404 - 2015-02-24

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