FDA inspection

Abon Biopharm (Hangzhou) Co., Ltd.: FDA inspection ending Jul 10, 2012

FDA inspection 792168 · No Action Indicated (NAI) · Hangzhou

Key facts

Inspection ID 792168
Firm Abon Biopharm (Hangzhou) Co., Ltd.
FEI number 3005641941
Address #198, #12 Street East, Hangzhou, Economic & Tech. Development Area
City Hangzhou
Country China
Fiscal year 2012
Inspection end date Jul 10, 2012
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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