FDA inspection

AMO (Hangzhou) Co., Ltd.: FDA inspection ending Jul 2, 2019

FDA inspection 1096712 · Voluntary Action Indicated (VAI) · Hangzhou

Key facts

Inspection ID 1096712
Firm AMO (Hangzhou) Co., Ltd.
FEI number 3004178847
Address No. 200 4th Avenue, Economic & Technological Development Zone
City Hangzhou
Country China
Fiscal year 2019
Inspection end date Jul 2, 2019
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 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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