FDA inspection

Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd: FDA inspection ending Mar 13, 2014

FDA inspection 872735 · Voluntary Action Indicated (VAI) · Jinhua

Key facts

Inspection ID 872735
Firm Zhejiang Apeloa Tospo Pharmaceuticals Co., Ltd
FEI number 3008259952
Address 519 Jiangnan Rd, Dongyang
City Jinhua
Country China
Fiscal year 2014
Inspection end date Mar 13, 2014
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes 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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