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FDA Inspection
•CorePharma, LLC•January 20, 2010

CorePharma, LLC – FDA Inspection, Jan 20, 2010

Record Details

This FDA Inspection record concerns CorePharma, LLC, with an inspection on January 20, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
CorePharma, LLC
Inspection Date
January 20, 2010
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 7e1b04c1-8d33-4fd2-9b0f-e1a3846a33e5

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
636223
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of CorePharma, LLC

13
DateClassificationOfficeProject area
August 28, 2025NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
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
View all 13 other inspections on the company page
Other documents for CorePharma, LLC
  • FDA Inspection 1280399 - 2025-08-28
  • FDA Inspection 1240419 - 2024-09-12
  • FDA Inspection 1087306 - 2019-03-29
  • FDA Inspection 1029942 - 2017-10-13
  • FDA Inspection 980585 - 2016-08-11

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