FDA Inspection 1265344 — Zhejiang Yongtai Pharmaceutical Co. Ltd

Zhejiang Yongtai Pharmaceutical Co. Ltd — FEI 3008828051

The FDA completed an inspection of Zhejiang Yongtai Pharmaceutical Co. Ltd on March 14, 2025 in Linhai. 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 14, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Linhai (China)