FDA inspection

Shenzhen Hepalink Pharmaceutical Group Co., Ltd.: FDA inspection ending Sep 16, 2021

FDA inspection 1153206 · No Action Indicated (NAI) · Shenzhen

Key facts

Inspection ID 1153206
Firm Shenzhen Hepalink Pharmaceutical Group Co., Ltd.
FEI number 3014772595
Address Building Ii, No. 1 Rongtian South; Kengzi Sub-District
City Shenzhen
Fiscal year 2021
Inspection end date Sep 16, 2021
Classification No Action Indicated (NAI)
Project area Generic Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • None 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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