FDA inspection

Arctic Biomaterials Oy: FDA inspection ending Jun 5, 2025

FDA inspection 1276438 · No Action Indicated (NAI) · Tampere

Key facts

Inspection ID 1276438
Firm Arctic Biomaterials Oy
FEI number 3015780293
Address Region Of Tampere, Arvo Ylpon Katu 41
City Tampere
Country Finland
Fiscal year 2025
Inspection end date Jun 5, 2025
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