FDA inspection

Interrad Medical Inc: FDA inspection ending Oct 30, 2019

FDA inspection 1121017 · Voluntary Action Indicated (VAI) · Minneapolis, MN

Key facts

Inspection ID 1121017
Firm Interrad Medical Inc
FEI number 3007795799
Address 181 Cheshire Ln N
City Minneapolis
State MN
ZIP 55441-5467
Fiscal year 2020
Inspection end date Oct 30, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical 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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