FDA inspection

Shenzhen Hepalink Pharmaceutical Group Co., Ltd.: FDA inspection ending Jun 13, 2025

FDA inspection 1276175 · Voluntary Action Indicated (VAI) · Shenzhen

Key facts

Inspection ID 1276175
Firm Shenzhen Hepalink Pharmaceutical Group Co., Ltd.
FEI number 3014772595
Address No. 1 Rongtian Road, Longgang District
City Shenzhen
Country China
Fiscal year 2025
Inspection end date Jun 13, 2025
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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