FDA inspection

Jacobson Resonance Enterprises, Inc.: FDA inspection ending Sep 5, 2002

FDA inspection 236478 · Voluntary Action Indicated (VAI) · Boynton Beach, FL

Key facts

Inspection ID 236478
Firm Jacobson Resonance Enterprises, Inc.
FEI number 3001452807
Address 8200 S Jog Rd Ste 100
City Boynton Beach
State FL
ZIP 33472-2981
Fiscal year 2002
Inspection end date Sep 5, 2002
Classification Voluntary Action Indicated (VAI)
Project area Product Evaluation: Med 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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