FDA inspection

Xellia (Taizhou) Pharmaceuticals Co., Ltd.: FDA inspection ending Jul 3, 2026

FDA inspection 1330508 · No Action Indicated (NAI) · Taizhou

Key facts

Inspection ID 1330508
Firm Xellia (Taizhou) Pharmaceuticals Co., Ltd.
FEI number 3007422723
City Taizhou
Country China
Fiscal year 2026
Inspection end date Jul 3, 2026
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

Browse all FDA inspections