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FDA Inspection
•Tianjin Zhongan Pharmaceutical Co., Ltd.•September 27, 2013

Tianjin Zhongan Pharmaceutical Co., Ltd. – FDA Inspection, Sep 27, 2013

Record Details

This FDA Inspection record concerns Tianjin Zhongan Pharmaceutical Co., Ltd., with an inspection on September 27, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Tianjin Zhongan Pharmaceutical Co., Ltd.
Inspection Date
September 27, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 86e3ccbf-4fea-4a10-bb77-98dea07bee72

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
851023
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Tianjin Zhongan Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
October 23, 2025NAICenter for Food Safety and Applied NutritionFoodborne Biological Hazards
February 2, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 24, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Tianjin Zhongan Pharmaceutical Co., Ltd.
  • FDA Inspection 1289190 - 2025-10-23
  • FDA Inspection 956512 - 2016-02-02
  • FDA Inspection 672160 - 2010-06-24

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