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FDA Inspection
•Hikma Pharmaceuticals USA INC.•January 17, 2025

Hikma Pharmaceuticals USA INC. – FDA Inspection, Jan 17, 2025

Record Details

This FDA Inspection record concerns Hikma Pharmaceuticals USA INC., with an inspection on January 17, 2025, issued by the Cincinnati District Office, covering human drugs.

Company
Hikma Pharmaceuticals USA INC.
Inspection Date
January 17, 2025
Product Type
Human Drugs
Office
Cincinnati District Office
People
  • D'Arbra R. Blankenship (Issuing Officer)
  • Kathryn L. Suttling (Company Rep)
View Company Profile

ID · be288e60-3b18-493f-bcd2-c5d2f1ca4059

Inspection Facts

Inspection number
1238509
FDA center
Human Drugs

Other FDA inspections of Hikma Pharmaceuticals USA INC.

27
DateClassificationOfficeProject area
September 18, 2026Not classifiedCincinnati District Office
April 30, 2026NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 23, 2024NAICompliance: Devices
September 15, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 22, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 27 other inspections on the company page
Other documents for Hikma Pharmaceuticals USA INC.
  • FDA Inspection 1285748 - 2026-09-18
  • FDA Inspection 1303412 - 2026-04-30
  • FDA Inspection 1243797 - 2024-07-23
  • FDA Inspection 1182363 - 2022-09-15
  • FDA Inspection 1113855 - 2019-11-22

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