FDA inspection

Icare Finland Oy: FDA inspection ending Apr 22, 2015

FDA inspection 927346 · Voluntary Action Indicated (VAI) · Vantaa

Key facts

Inspection ID 927346
Firm Icare Finland Oy
FEI number 3005324856
Address Ayritie 22
City Vantaa
Country Finland
Fiscal year 2015
Inspection end date Apr 22, 2015
Classification Voluntary Action Indicated (VAI)
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