FDA inspection

Xellia (Taizhou) Pharmaceuticals Co., Ltd.: FDA inspection ending Sep 20, 2012

FDA inspection 801705 · No Action Indicated (NAI) · Taizhou

Key facts

Inspection ID 801705
Firm Xellia (Taizhou) Pharmaceuticals Co., Ltd.
FEI number 3007422723
Address 108 Binhailu, Jiaojiang
City Taizhou
Country China
Fiscal year 2012
Inspection end date Sep 20, 2012
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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