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FDA Inspection
•Repligen Corporation•February 8, 2024

Repligen Corporation – FDA Inspection, Feb 8, 2024

Record Details

This FDA Inspection record concerns Repligen Corporation, with an inspection on February 8, 2024, issued by the Dallas District Office, covering medical devices & rad health.

Company
Repligen Corporation
Inspection Date
February 8, 2024
Product Type
Medical Devices & Rad Health
Office
Dallas District Office
View Company Profile

ID · b376683b-7c2d-4895-9916-e29c25df34ba

Inspection Facts

Inspection number
1230139
FDA center
Medical Devices & Rad Health
Outcome
Form 483 issued

Other FDA inspections of Repligen Corporation

4
DateClassificationOfficeProject area
January 25, 2018Not classifiedDallas District Office
November 4, 2013VAICenter for Devices and Radiological HealthCompliance: Devices
August 7, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
March 26, 2009NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Repligen Corporation
  • FDA Inspection 1041140 - 2018-01-25
  • FDA Inspection 853838 - 2013-11-04
  • FDA Inspection 843335 - 2013-08-07
  • FDA Inspection 572949 - 2009-03-26

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