FDA inspection

Aionex, Inc.: FDA inspection ending Jun 9, 2014

FDA inspection 882505 · No Action Indicated (NAI) · Madison, TN

Key facts

Inspection ID 882505
Firm Aionex, Inc.
FEI number 3005627440
Address 122 Cude Ln
City Madison
State TN
ZIP 37115
Country United States
Fiscal year 2014
Inspection end date Jun 9, 2014
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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

Browse all FDA inspections