FDA inspection

Zhejiang Orient Gene Biotech: FDA inspection ending Jan 17, 2014

FDA inspection 868769 · No Action Indicated (NAI) · Huzhou

Key facts

Inspection ID 868769
Firm Zhejiang Orient Gene Biotech
FEI number 3008517993
Address Ji Er Road Jiankang Industrial Area, Anji Economic Development Zone
City Huzhou
Country China
Fiscal year 2014
Inspection end date Jan 17, 2014
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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