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FDA Inspection
•Vertex Pharmaceuticals Incorporated•March 3, 2026

Vertex Pharmaceuticals Incorporated – FDA Inspection, Mar 3, 2026

Record Details

This FDA Inspection record concerns Vertex Pharmaceuticals Incorporated, with an inspection on March 3, 2026, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Vertex Pharmaceuticals Incorporated
Inspection Date
March 3, 2026
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Armen H. Youssoufian (Issuing Officer)
  • Edmund F. Mrak (FDA Associated Person)
View Company Profile

ID · bc146f43-1e81-4339-a15b-d826e903c323

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1306258
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Vertex Pharmaceuticals Incorporated

14
DateClassificationOfficeProject area
July 31, 2026Not classifiedNew England District Office
August 1, 2024NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
May 4, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 19, 2022NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
October 5, 2017NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
View all 14 other inspections on the company page
Other documents for Vertex Pharmaceuticals Incorporated
  • FDA Inspection 1333028 - 2026-07-31
  • FDA Inspection 1246447 - 2024-08-01
  • FDA Inspection 1205834 - 2023-05-04
  • FDA Inspection 1180001 - 2022-08-19
  • FDA Inspection 1029564 - 2017-10-05

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