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FDA Inspection
•Zhejiang Huahai Pharmaceutical Co., Ltd.•May 31, 2019

Zhejiang Huahai Pharmaceutical Co., Ltd. – FDA Inspection, May 31, 2019

Record Details

This FDA Inspection record concerns Zhejiang Huahai Pharmaceutical Co., Ltd., with an inspection on May 31, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Huahai Pharmaceutical Co., Ltd.
Inspection Date
May 31, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Jonathan W. Chapman (Company Rep)
  • Zedong Dong (FDA Associated Person)
View Company Profile

ID · 2b5b7233-044f-42f2-ac3f-00e6696bfc49

Inspection Facts

Official Action Indicated (OAI)

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

Inspection number
1093250
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Zhejiang Huahai Pharmaceutical Co., Ltd.

10
DateClassificationOfficeProject area
April 24, 2026Not classifiedOffice of Inspections and Investigations
January 24, 2025OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 2, 2021NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 28, 2019Not classifiedOffice of Inspections and Investigations
January 26, 2018Not classifiedOffice of Inspections and Investigations
View all 10 other inspections on the company page
Other documents for Zhejiang Huahai Pharmaceutical Co., Ltd.
  • FDA Inspection 1319736 - 2026-04-24
  • FDA Inspection 1259818 - 2025-01-24
  • FDA Inspection 1149252 - 2021-07-02
  • FDA Inspection 1094941 - 2019-06-28
  • FDA Inspection 1042575 - 2018-01-26

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