FDA inspection

Murata Vios, Inc.: FDA inspection ending Dec 11, 2024

FDA inspection 1257019 · Voluntary Action Indicated (VAI) · Woodbury, MN

Key facts

Inspection ID 1257019
Firm Murata Vios, Inc.
FEI number 3015328411
Address 700 Commerce Dr Ste 190
City Woodbury
State MN
ZIP 55125
Country United States
Fiscal year 2025
Inspection end date Dec 11, 2024
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 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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