FDA inspection

NIOX Inc: FDA inspection ending Nov 5, 2010

FDA inspection 696735 · Voluntary Action Indicated (VAI) · Morrisville, NC

Key facts

Inspection ID 696735
Firm NIOX Inc
FEI number 3006173825
Address 1100 Perimeter Park Dr Ste 114
City Morrisville
State NC
ZIP 27560
Country United States
Fiscal year 2011
Inspection end date Nov 5, 2010
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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

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