FDA Inspection 786950 — Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
The FDA completed an inspection of Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd on May 17, 2012 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
- May 17, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Hangzhou (China)