FDA Inspection 1114388 — Luoyang MuChun Pharmaceutical Co., Ltd.
The FDA completed an inspection of Luoyang MuChun Pharmaceutical Co., Ltd. on Dec 6, 2019 in Yanshi City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 6, 2019
- Fiscal Year
- 2020
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Yanshi City (China)