FDA inspection

Lutonix Inc.: FDA inspection ending Jun 25, 2013

FDA inspection 838849 · No Action Indicated (NAI) · Tempe, AZ

Key facts

Inspection ID 838849
Firm Lutonix Inc.
FEI number 3006513822
Address 9409 Science Center Dr
City Tempe
State AZ
ZIP 85281
Country United States
Fiscal year 2013
Inspection end date Jun 25, 2013
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

Browse all FDA inspections