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FDA Inspection
•Sinopharm Weiqida Pharmaceutical Co. Ltd.•May 25, 2023

Sinopharm Weiqida Pharmaceutical Co. Ltd. – FDA Inspection, May 25, 2023

Record Details

This FDA Inspection record concerns Sinopharm Weiqida Pharmaceutical Co. Ltd., with an inspection on May 25, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Sinopharm Weiqida Pharmaceutical Co. Ltd.
Inspection Date
May 25, 2023
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Tonia F. Bernard
View Company Profile

ID · b4ad5182-3f8a-40cb-afd1-d9e89487b422

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1209420
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Sinopharm Weiqida Pharmaceutical Co. Ltd.

2
DateClassificationOfficeProject area
July 21, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 1, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Sinopharm Weiqida Pharmaceutical Co. Ltd.
  • FDA Inspection 1028876 - 2017-07-21
  • FDA Inspection 932412 - 2015-05-01

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