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FDA Inspection
•Guilin China Resources Tianhe Pharmaceutical Co., Ltd.•March 28, 2025

Guilin China Resources Tianhe Pharmaceutical Co., Ltd. – FDA Inspection, Mar 28, 2025

Record Details

This FDA Inspection record concerns Guilin China Resources Tianhe Pharmaceutical Co., Ltd., with an inspection on March 28, 2025, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Guilin China Resources Tianhe Pharmaceutical Co., Ltd.
Inspection Date
March 28, 2025
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jonathan G. Matrisciano (FDA Associated Person)
View Company Profile

ID · 8e55f59b-b213-4c68-9f30-c9810bec4d5e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1268372
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Guilin China Resources Tianhe Pharmaceutical Co., Ltd.

1
DateClassificationOfficeProject area
January 11, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Guilin China Resources Tianhe Pharmaceutical Co., Ltd.
  • FDA Inspection 1078047 - 2019-01-11

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