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FDA Inspection
•Yicheng Goto Pharmaceuticals Co., Ltd•September 14, 2017

Yicheng Goto Pharmaceuticals Co., Ltd – FDA Inspection, Sep 14, 2017

Record Details

This FDA Inspection record concerns Yicheng Goto Pharmaceuticals Co., Ltd, with an inspection on September 14, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Yicheng Goto Pharmaceuticals Co., Ltd
Inspection Date
September 14, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Meisha R. Sampson (Issuing Officer)
View Company Profile

ID · c7588f1e-3a82-4d0b-b0fd-2a42153aa64f

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1026312
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Yicheng Goto Pharmaceuticals Co., Ltd

2
DateClassificationOfficeProject area
September 4, 2014OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 15, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Yicheng Goto Pharmaceuticals Co., Ltd
  • FDA Inspection 894198 - 2014-09-04
  • FDA Inspection 748983 - 2011-09-15

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