FDA Inspection
Liuzhou Liangmianzhen (LMZ) Co., Ltd.Liuzhou Liangmianzhen (LMZ) Co., Ltd. – FDA Inspection, Jul 5, 2019
Record Details
This FDA Inspection record concerns Liuzhou Liangmianzhen (LMZ) Co., Ltd., with an inspection on July 5, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 36d09f59-399f-4b1f-af03-14ceb7e9d040
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1099631
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Liuzhou Liangmianzhen (LMZ) Co., Ltd.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 22, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Liuzhou Liangmianzhen (LMZ) Co., Ltd.
- FDA Inspection 1236678 - 2024-03-22
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