FDA inspection

Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd: FDA inspection ending Oct 24, 2025

FDA inspection 1293216 · No Action Indicated (NAI) · Jinhua

Key facts

Inspection ID 1293216
Firm Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd
FEI number 3008259952
Address 519 Jiang Shanbeicun, Hengdianzhen Dongyang
City Jinhua
Country China
Fiscal year 2026
Inspection end date Oct 24, 2025
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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