FDA Inspection 1254673 — Shijiazhuang Lonzeal Pharmaceuticals Co., Ltd

Shijiazhuang Lonzeal Pharmaceuticals Co., Ltd — FEI 3010066204

The FDA completed an inspection of Shijiazhuang Lonzeal Pharmaceuticals Co., Ltd on October 18, 2024 in Shijiazhuang. 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 18, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shijiazhuang (China)