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FDA Inspection
•Zhejiang Better Pharmaceuticals Co., Ltd.•January 20, 2017

Zhejiang Better Pharmaceuticals Co., Ltd. – FDA Inspection, Jan 20, 2017

Record Details

This FDA Inspection record concerns Zhejiang Better Pharmaceuticals Co., Ltd., with an inspection on January 20, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Better Pharmaceuticals Co., Ltd.
Inspection Date
January 20, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Roger F. Zabinski (FDA Associated Person)
  • Yasamin Ameri (FDA Associated Person)
View Company Profile

ID · 7f3f48bd-c3a3-4dcb-8a6c-b354f1364c91

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1005236
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Zhejiang Better Pharmaceuticals Co., Ltd.

1
DateClassificationOfficeProject area
September 26, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Better Pharmaceuticals Co., Ltd.
  • FDA Inspection 1252973 - 2024-09-26

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