FDA Inspection 872735 — Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd
The FDA completed an inspection of Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd on March 13, 2014 in Jinhua. 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 13, 2014
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Jinhua (China)