FDA inspection

Liuzhou Liangmianzhen (LMZ) Co., Ltd.: FDA inspection ending Mar 22, 2024

FDA inspection 1236678 · Voluntary Action Indicated (VAI) · Liuzhou

Key facts

Inspection ID 1236678
Firm Liuzhou Liangmianzhen (LMZ) Co., Ltd.
FEI number 3002895902
Address 282 East Ring Rd
City Liuzhou
Country China
Fiscal year 2024
Inspection end date Mar 22, 2024
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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