FDA Inspection 1236678 — Liuzhou Liangmianzhen (LMZ) Co., Ltd.
The FDA completed an inspection of Liuzhou Liangmianzhen (LMZ) Co., Ltd. on March 22, 2024 in Liuzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 22, 2024
- Fiscal Year
- 2024
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Liuzhou (China)