FDA inspection

Shenzhen Hepalink Pharmaceutical Co., Ltd.: FDA inspection ending Apr 28, 2005

FDA inspection 381245 · Voluntary Action Indicated (VAI) · Shenzhen

Key facts

Inspection ID 381245
Firm Shenzhen Hepalink Pharmaceutical Co., Ltd.
FEI number 3002808210
Address Songpingshan, 21 Langshan Road; Nanshan District
City Shenzhen
Fiscal year 2005
Inspection end date Apr 28, 2005
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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