# Zhejiang Liaoyuan Pharmaceutical Co., Ltd. – FDA Inspection, Jun 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/zhejiang-liaoyuan-pharmaceutical-co-ltd/9755a0a7-acdb-40c0-92a1-b296912c46cc
Source feed: FDA_Inspections

> FDA inspection 1019163 of Zhejiang Liaoyuan Pharmaceutical Co., Ltd., June 09, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1019163
- Company Name: Zhejiang Liaoyuan Pharmaceutical Co., Ltd.
- Inspection Date: 2017-06-09
- 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

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- [FDA Inspection 1217646 - 2023-08-25](https://www.keypedia.com/records/fda_inspections/zhejiang-liaoyuan-pharmaceutical-co-ltd/e8db4578-8be6-4f31-bde9-486ef7e45a47)

## Related Officers

- [Robert J. Martin](https://www.keypedia.com/people/robert-j-martin/8bd5c75a-ec53-4ae5-9739-a39489686cae)

Company: https://www.keypedia.com/companies/zhejiang-liaoyuan-pharmaceutical-co-ltd/5e084d5d-74f8-495e-960b-072dabe6a6a6

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