FDA inspection

NEURAXIS, INC: FDA inspection ending Jun 6, 2018

FDA inspection 1055858 · No Action Indicated (NAI) · Carmel, IN

Key facts

Inspection ID 1055858
Firm NEURAXIS, INC
FEI number 3009293069
Address 829 S Adams St
City Carmel
State IN
ZIP 46032
Country United States
Fiscal year 2018
Inspection end date Jun 6, 2018
Classification No Action Indicated (NAI)
Project area Bioresearch Monitoring
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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