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FDA Inspection
•Chongqing Carelife Pharmaceutical Co., Ltd.•November 30, 2017

Chongqing Carelife Pharmaceutical Co., Ltd. – FDA Inspection, Nov 30, 2017

Record Details

This FDA Inspection record concerns Chongqing Carelife Pharmaceutical Co., Ltd., with an inspection on November 30, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Chongqing Carelife Pharmaceutical Co., Ltd.
Inspection Date
November 30, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Christopher T. Middendorf (FDA Associated Person)
  • Peter E. Baker (FDA Associated Person)
View Company Profile

ID · a3d54cae-08f1-4200-85a5-c3844dbf7dde

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1035442
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Chongqing Carelife Pharmaceutical Co., Ltd.

5
DateClassificationOfficeProject area
March 28, 2025Not classifiedOffice of Inspections and Investigations
July 19, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 19, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 18, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 30, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Chongqing Carelife Pharmaceutical Co., Ltd.
  • FDA Inspection 1268964 - 2025-03-28
  • FDA Inspection 1098996 - 2019-07-19
  • FDA Inspection 970028 - 2016-05-19
  • FDA Inspection 851858 - 2013-10-18
  • FDA Inspection 684797 - 2010-07-30

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