FDA Inspection 985170 — Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
The FDA completed an inspection of Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd on July 28, 2016 in Hangzhou. 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
- July 28, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Hangzhou (China)