FDA inspection

ScandiDos AB: FDA inspection ending Aug 28, 2019

FDA inspection 1128932 · Voluntary Action Indicated (VAI) · Uppsala

Key facts

Inspection ID 1128932
Firm ScandiDos AB
FEI number 3005596716
Address Dag Hammarskjolds Vag 52a
City Uppsala
Fiscal year 2019
Inspection end date Aug 28, 2019
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None 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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