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FDA Inspection
•Hebei Jiheng Pharmaceutical Co., Ltd.•June 21, 2024

Hebei Jiheng Pharmaceutical Co., Ltd. – FDA Inspection, Jun 21, 2024

Record Details

This FDA Inspection record concerns Hebei Jiheng Pharmaceutical Co., Ltd., with an inspection on June 21, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Hebei Jiheng Pharmaceutical Co., Ltd.
Inspection Date
June 21, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • WenNing Chan (Issuing Officer)
View Company Profile

ID · eb5a8785-f429-4287-96e4-6c3699556d88

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1243675
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Hebei Jiheng Pharmaceutical Co., Ltd.

2
DateClassificationOfficeProject area
August 28, 2026Not classifiedOffice of Inspections and Investigations
June 9, 2023Not classifiedOffice of Inspections and Investigations
Other documents for Hebei Jiheng Pharmaceutical Co., Ltd.
  • FDA Inspection 1337158 - 2026-08-28
  • FDA Inspection 1211399 - 2023-06-09

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