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FDA Inspection
•Rechon Life Science AB•March 17, 2023

Rechon Life Science AB – FDA Inspection, Mar 17, 2023

Record Details

This FDA Inspection record concerns Rechon Life Science AB, with an inspection on March 17, 2023, issued by the Office of Inspections and Investigations.

Company
Rechon Life Science AB
Inspection Date
March 17, 2023
Office
Office of Inspections and Investigations
People
  • Lisa L. Flores (Investigator)
  • Monica E. Murie (Investigator)
View Company Profile

ID · 3d26d3f2-e239-49fc-bdc7-693e67114bac

Inspection Facts

Inspection number
1201600
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Rechon Life Science AB

7
DateClassificationOfficeProject area
September 6, 2024OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 27, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 29, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 2, 2016NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
April 29, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Rechon Life Science AB
  • FDA Inspection 1251480 - 2024-09-06
  • FDA Inspection 1125627 - 2019-11-27
  • FDA Inspection 1060687 - 2018-06-29
  • FDA Inspection 983550 - 2016-06-02
  • FDA Inspection 969057 - 2016-04-29

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