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FDA Inspection
•CoreRX Inc.•June 14, 2019

CoreRX Inc. – FDA Inspection, Jun 14, 2019

Record Details

This FDA Inspection record concerns CoreRX Inc., with an inspection on June 14, 2019, issued by the Florida District Office, covering biologics.

Company
CoreRX Inc.
Inspection Date
June 14, 2019
Product Type
Biologics
Office
Florida District Office
Person
  • Laura Fontan (Company Rep)
View Company Profile

ID · eca31204-eefa-4624-9cb1-e52a10251f01

Inspection Facts

Inspection number
1105141
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of CoreRX Inc.

8
DateClassificationOfficeProject area
February 26, 2026Not classifiedFlorida District OfficeDrug Quality Assurance
March 20, 2025Not classifiedFlorida District OfficeVaccine, Allergenic, and Live Biotherapeutic Products
August 13, 2021NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 6, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 21, 2019VAIFlorida District OfficeGeneric Drug Evaluation
View all 8 other inspections on the company page
Other documents for CoreRX Inc.
  • FDA Inspection 1304588 - 2026-02-26
  • FDA Inspection 1264769 - 2025-03-20
  • FDA Inspection 1151289 - 2021-08-13
  • FDA Inspection 1119912 - 2020-03-06
  • FDA Inspection 1094038 - 2019-06-21

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