FDA inspection

Iradimed Corporation: FDA inspection ending Jul 18, 2016

FDA inspection 983093 · Voluntary Action Indicated (VAI) · orlando, FL

Key facts

Inspection ID 983093
Firm Iradimed Corporation
FEI number 3005053560
Address 1025 Willa Springs Dr
City orlando
State FL
ZIP 32826
Country United States
Fiscal year 2016
Inspection end date Jul 18, 2016
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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