FDA inspection

Chengdu Shengnuo Biopharm Co., Ltd.: FDA inspection ending Sep 8, 2023

FDA inspection 1219460 · Voluntary Action Indicated (VAI) · Chengdu

Key facts

Inspection ID 1219460
Firm Chengdu Shengnuo Biopharm Co., Ltd.
FEI number 3006257504
Address Section 1, Gongye Avenue, Dayi County
City Chengdu
Country China
Fiscal year 2023
Inspection end date Sep 8, 2023
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
  • Yes 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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