FDA inspection

Palodex Group Oy: FDA inspection ending Sep 4, 2015

FDA inspection 944319 · Voluntary Action Indicated (VAI) · Tuusula

Key facts

Inspection ID 944319
Firm Palodex Group Oy
FEI number 3005383085
Address Nahkelantie 160
City Tuusula
Country Finland
Fiscal year 2015
Inspection end date Sep 4, 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