FDA Inspection 1293216 — Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd

Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd — FEI 3008259952

The FDA completed an inspection of Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd on October 24, 2025 in Jinhua. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 24, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jinhua (China)