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FDA Inspection
•Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd.•September 29, 2016

Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd. – FDA Inspection, Sep 29, 2016

Record Details

This FDA Inspection record concerns Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd., with an inspection on September 29, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd.
Inspection Date
September 29, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 2c9eeacf-cfd3-4e12-8bff-b5a11cb44312

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
989767
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd.

4
DateClassificationOfficeProject area
March 21, 2025Not classifiedOffice of Inspections and Investigations
August 2, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 2, 2018Not classifiedOffice of Inspections and Investigations
August 29, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Teva Pharmaceutical and Chemical (Hangzhou) Co. Ltd.
  • FDA Inspection 1266237 - 2025-03-21
  • FDA Inspection 1155300 - 2019-08-02
  • FDA Inspection 1041618 - 2018-02-02
  • FDA Inspection 854635 - 2013-08-29

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