FDA inspection

Jacobson Resonance Enterprises, Inc.: FDA inspection ending Sep 15, 2000

FDA inspection 39365 · Official Action Indicated (OAI) · Boynton Beach, FL

Key facts

Inspection ID 39365
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 2000
Inspection end date Sep 15, 2000
Classification Official Action Indicated (OAI)
Project area Product Evaluation: Med Devices
Product type Devices
Warning letter UCM069254

At a glance

  • None Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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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