FDA inspection

Arjo (Suzhou) Co., Ltd.: FDA inspection ending Nov 24, 2011

FDA inspection 756296 · No Action Indicated (NAI) · Suzhou

Key facts

Inspection ID 756296
Firm Arjo (Suzhou) Co., Ltd.
FEI number 3005619970
Address NO 158 Fangzhou Rd, SIP, Zhong Xin Gongyeyuanqu
City Suzhou
Country China
Fiscal year 2012
Inspection end date Nov 24, 2011
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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

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