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FDA Inspection
•BioMarin International Limited•May 2, 2017

BioMarin International Limited – FDA Inspection, May 2, 2017

Record Details

This FDA Inspection record concerns BioMarin International Limited, with an inspection on May 2, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
BioMarin International Limited
Inspection Date
May 2, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Bo Chi (Issuing Officer)
  • Kathleen R. Jones (Company Rep)
View Company Profile

ID · 041c9fb4-05a5-4075-a7c4-7a812bef61c2

Inspection Facts

Inspection number
1010352
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of BioMarin International Limited

5
DateClassificationOfficeProject area
December 13, 2024Not classifiedOffice of Inspections and Investigations
February 16, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 7, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 27, 2017Not classifiedOffice of Inspections and Investigations
July 15, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for BioMarin International Limited
  • FDA Inspection 1263534 - 2024-12-13
  • FDA Inspection 1243568 - 2024-02-16
  • FDA Inspection 1123865 - 2018-12-07
  • FDA Inspection 1030194 - 2017-10-27
  • FDA Inspection 981531 - 2016-07-15

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