FDA inspection

Joyang Laboratories: FDA inspection ending May 5, 2017

FDA inspection 1021129 · Voluntary Action Indicated (VAI) · Yancheng

Key facts

Inspection ID 1021129
Firm Joyang Laboratories
FEI number 3008639692
Address Haidu North Road, Sheyang Economic Development Zone
City Yancheng
Country China
Fiscal year 2017
Inspection end date May 5, 2017
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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