FDA inspection

BeiGene (Suzhou) Co., Ltd.: FDA inspection ending Aug 28, 2019

FDA inspection 1103267 · No Action Indicated (NAI) · Suzhou

Key facts

Inspection ID 1103267
Firm BeiGene (Suzhou) Co., Ltd.
FEI number 3014150588
Address Bldg 6 4th Floor, 218 Sangtian St
City Suzhou
Fiscal year 2019
Inspection end date Aug 28, 2019
Classification No Action Indicated (NAI)
Project area New 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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