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FDA Inspection
•Zhejiang Chiral Medicine Chemicals Co., Ltd.•September 12, 2019

Zhejiang Chiral Medicine Chemicals Co., Ltd. – FDA Inspection, Sep 12, 2019

Record Details

This FDA Inspection record concerns Zhejiang Chiral Medicine Chemicals Co., Ltd., with an inspection on September 12, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Chiral Medicine Chemicals Co., Ltd.
Inspection Date
September 12, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jeffrey P. Raimondi (Investigator)
View Company Profile

ID · f8d5df85-1ad0-4c18-86d1-85d266639f4f

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1106711
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Zhejiang Chiral Medicine Chemicals Co., Ltd.

5
DateClassificationOfficeProject area
March 14, 2025Not classifiedOffice of Inspections and Investigations
October 13, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 11, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 29, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 19, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Chiral Medicine Chemicals Co., Ltd.
  • FDA Inspection 1267769 - 2025-03-14
  • FDA Inspection 1036694 - 2017-10-13
  • FDA Inspection 983665 - 2016-08-11
  • FDA Inspection 817858 - 2013-01-29
  • FDA Inspection 750355 - 2011-08-19

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