FDA inspection

Lumis Global Pharmaceuticals Co. Ltd.: FDA inspection ending Sep 28, 2016

FDA inspection 988256 · Official Action Indicated (OAI) · Wuhan

Key facts

Inspection ID 988256
Firm Lumis Global Pharmaceuticals Co. Ltd.
FEI number 3010280514
Address Huishang Mansion Unit 305, 2 Wudayuan Rd Donghu Ntdz
City Wuhan
Country China
Fiscal year 2016
Inspection end date Sep 28, 2016
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs
Warning letter 516043

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes 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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