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

Source: https://www.keypedia.com/records/fda_inspections/guilin-china-resources-tianhe-pharmaceutical-co-ltd/8e55f59b-b213-4c68-9f30-c9810bec4d5e
Source feed: FDA_Inspections

> FDA inspection 1268372 of Guilin China Resources Tianhe Pharmaceutical Co., Ltd., March 28, 2025. Classification: Voluntary Action Indicated (VAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1268372
- Company Name: Guilin China Resources Tianhe Pharmaceutical Co., Ltd.
- Inspection Date: 2025-03-28
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Center: Human Drugs
- Office Name: Center for Drug Evaluation and Research
- Citation Count: 0

## Related Documents

- [FDA Inspection 1078047 - 2019-01-11](https://www.keypedia.com/records/fda_inspections/guilin-china-resources-tianhe-pharmaceutical-co-ltd/497581b2-9e0b-4df5-9e17-370621d1acb6)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jonathan-g-matrisciano/17e5bce2-75a6-4182-925d-b94b42763dd2)

Company: https://www.keypedia.com/companies/guilin-china-resources-tianhe-pharmaceutical-co-ltd/a267013f-a39d-4270-a42a-8ba4706e6b86

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c