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FDA Inspection
•Lonza Guangzhou Pharmaceutical Ltd.•October 31, 2025

Lonza Guangzhou Pharmaceutical Ltd. – FDA Inspection, Oct 31, 2025

Record Details

This FDA Inspection record concerns Lonza Guangzhou Pharmaceutical Ltd., with an inspection on October 31, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Lonza Guangzhou Pharmaceutical Ltd.
Inspection Date
October 31, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • David V. Ward
  • Jose M. Cayuela (FDA Associated Person)
  • Wang Liquan (Issuing Officer)
View Company Profile

ID · 6df8e4c7-99a4-4669-85d6-191812ef13ce

Inspection Facts

Inspection number
1292806
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Lonza Guangzhou Pharmaceutical Ltd.

4
DateClassificationOfficeProject area
December 14, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 19, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 23, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 4, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Lonza Guangzhou Pharmaceutical Ltd.
  • FDA Inspection 1077023 - 2018-12-14
  • FDA Inspection 981011 - 2016-08-19
  • FDA Inspection 846043 - 2013-08-23
  • FDA Inspection 709669 - 2010-12-04

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