FDA inspection

Unimicro Medical Systems (Shenzhen) Co., Ltd.: FDA inspection ending Mar 3, 2023

FDA inspection 1199692 · Voluntary Action Indicated (VAI) · Shenzhen

Key facts

Inspection ID 1199692
Firm Unimicro Medical Systems (Shenzhen) Co., Ltd.
FEI number 3010806467
Address 201, Bldg 38, 101 Heshui Kou; Gongmingzhen Longgang
City Shenzhen
Country China
Fiscal year 2023
Inspection end date Mar 3, 2023
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

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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