# Liuzhou Liangmianzhen (LMZ) Co., Ltd. – FDA Inspection, Jul 5, 2019

Source: https://www.keypedia.com/records/fda_inspections/liuzhou-liangmianzhen-lmz-co-ltd/36d09f59-399f-4b1f-af03-14ceb7e9d040
Source feed: FDA_Inspections

> FDA inspection 1099631 of Liuzhou Liangmianzhen (LMZ) Co., Ltd., July 05, 2019. 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: 1099631
- Company Name: Liuzhou Liangmianzhen (LMZ) Co., Ltd.
- Inspection Date: 2019-07-05
- 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 1236678 - 2024-03-22

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/zhongren-wu/416f09a6-f225-4d23-a305-34f96a5c78f0)

Company: https://www.keypedia.com/companies/liuzhou-liangmianzhen-lmz-co-ltd/65235d99-a657-42fc-a43b-469f3c722a68

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