FDA Inspection 823594 — Anshi Pharmaceutical (Zhongshan) Inc.
The FDA completed an inspection of Anshi Pharmaceutical (Zhongshan) Inc. on October 31, 2012 in Zhongshan. 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
- October 31, 2012
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Zhongshan (China)