FDA inspection

Radscan Medical Equipment Inc: FDA inspection ending Sep 19, 2017

FDA inspection 1028553 · No Action Indicated (NAI) · Phoenix, AZ

Key facts

Inspection ID 1028553
Firm Radscan Medical Equipment Inc
FEI number 3004185485
Address 23910 N 19th Ave Ste B4-66
City Phoenix
State AZ
ZIP 85085
Country United States
Fiscal year 2017
Inspection end date Sep 19, 2017
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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