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FDA Inspection
•Hovione PharmaScience Limited•December 12, 2025

Hovione PharmaScience Limited – FDA Inspection, Dec 12, 2025

Record Details

This FDA Inspection record concerns Hovione PharmaScience Limited, with an inspection on December 12, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Hovione PharmaScience Limited
Inspection Date
December 12, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Andrew Le (FDA Associated Person)
  • Lillian S. Wu (Issuing Officer)
View Company Profile

ID · 463f880a-e0e1-4b40-9fda-8ec76b6f40b8

Inspection Facts

Inspection number
1298568
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Hovione PharmaScience Limited

4
DateClassificationOfficeProject area
July 20, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 20, 2016NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
January 30, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 24, 2009VAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
Other documents for Hovione PharmaScience Limited
  • FDA Inspection 1065839 - 2018-07-20
  • FDA Inspection 977551 - 2016-05-20
  • FDA Inspection 823144 - 2013-01-30
  • FDA Inspection 597922 - 2009-06-24

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