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FDA Inspection
•Zhengzhou Minzhong Pharmaceutical Co., Ltd.•May 11, 2017

Zhengzhou Minzhong Pharmaceutical Co., Ltd. – FDA Inspection, May 11, 2017

Record Details

This FDA Inspection record concerns Zhengzhou Minzhong Pharmaceutical Co., Ltd., with an inspection on May 11, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhengzhou Minzhong Pharmaceutical Co., Ltd.
Inspection Date
May 11, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Teresa I. Navas
View Company Profile

ID · 2c4d18ef-019a-469e-9b56-60eb85e24293

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1014502
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Zhengzhou Minzhong Pharmaceutical Co., Ltd.

1
DateClassificationOfficeProject area
April 23, 2018OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhengzhou Minzhong Pharmaceutical Co., Ltd.
  • FDA Inspection 1049988 - 2018-04-23

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