FDA inspection

Immersivetouch Inc: FDA inspection ending Jan 29, 2020

FDA inspection 1116352 · Voluntary Action Indicated (VAI) · Chicago, IL

Key facts

Inspection ID 1116352
Firm Immersivetouch Inc
FEI number 3014833795
Address 910 W Van Buren St Ste 715
City Chicago
State IL
ZIP 60607
Country United States
Fiscal year 2020
Inspection end date Jan 29, 2020
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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