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FDA Inspection
•Taizhou Xianju Pharmaceutical Co. Ltd.•March 31, 2017

Taizhou Xianju Pharmaceutical Co. Ltd. – FDA Inspection, Mar 31, 2017

Record Details

This FDA Inspection record concerns Taizhou Xianju Pharmaceutical Co. Ltd., with an inspection on March 31, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Taizhou Xianju Pharmaceutical Co. Ltd.
Inspection Date
March 31, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Tajah L. Blackburn (FDA Associated Person)
View Company Profile

ID · c928eb35-fe18-41ef-b120-6c5e93656bb3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1009605
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Taizhou Xianju Pharmaceutical Co. Ltd.

1
DateClassificationOfficeProject area
November 15, 2024NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Taizhou Xianju Pharmaceutical Co. Ltd.
  • FDA Inspection 1256835 - 2024-11-15

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