FDA inspection

Shenzhen Hepalink Pharmaceutical Co., Ltd.: FDA inspection ending Nov 26, 2008

FDA inspection 556264 · No Action Indicated (NAI) · Shenzhen

Key facts

Inspection ID 556264
Firm Shenzhen Hepalink Pharmaceutical Co., Ltd.
FEI number 3002808210
Address Songpingshan, 21 Langshan Road; Nanshan District
City Shenzhen
Country China
Fiscal year 2009
Inspection end date Nov 26, 2008
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

Browse all FDA inspections