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FDA Inspection
•Haimen Pharma Co., Ltd.•September 8, 2017

Haimen Pharma Co., Ltd. – FDA Inspection, Sep 8, 2017

Record Details

This FDA Inspection record concerns Haimen Pharma Co., Ltd., with an inspection on September 8, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Haimen Pharma Co., Ltd.
Inspection Date
September 8, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Anitha P. Govada (Company Rep)
  • Cheryl A. Clausen
View Company Profile

ID · f95ae01e-dca4-45bf-8b8c-cd748a6c732e

Inspection Facts

Inspection number
1027385
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Haimen Pharma Co., Ltd.

3
DateClassificationOfficeProject area
August 25, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 10, 2020NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 12, 2019VAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
Other documents for Haimen Pharma Co., Ltd.
  • FDA Inspection 1254733 - 2023-08-25
  • FDA Inspection 1115958 - 2020-01-10
  • FDA Inspection 1078088 - 2019-01-12

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