FDA inspection

Genicon, Inc.: FDA inspection ending Apr 21, 2015

FDA inspection 923674 · Voluntary Action Indicated (VAI) · Winter Park, FL

Key facts

Inspection ID 923674
Firm Genicon, Inc.
FEI number 3002590791
Address 6869 Stapoint Ct Ste 112
City Winter Park
State FL
ZIP 32792
Country United States
Fiscal year 2015
Inspection end date Apr 21, 2015
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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