FDA inspection

MEDTRONIC GRAND RAPIDS: FDA inspection ending Dec 15, 2025

FDA inspection 1296772 · Voluntary Action Indicated (VAI) · Grand Rapids, MI

Key facts

Inspection ID 1296772
Firm MEDTRONIC GRAND RAPIDS
FEI number 3003955307
Address 620 Watson St Sw
City Grand Rapids
State MI
ZIP 49504
Country United States
Fiscal year 2026
Inspection end date Dec 15, 2025
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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