FDA inspection

eNeura, Inc.: FDA inspection ending Jan 11, 2018

FDA inspection 1041913 · No Action Indicated (NAI) · West Palm Beach, FL

Key facts

Inspection ID 1041913
Firm eNeura, Inc.
FEI number 3008487930
Address 715 N Pastoria Ave
City West Palm Beach
State FL
ZIP 33405
Country United States
Fiscal year 2018
Inspection end date Jan 11, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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