FDA Inspection 1276424 — Inion Oy

Inion Oy — FEI 3003407235

The FDA completed an inspection of Inion Oy on Jun 3, 2025 in Tampere. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 3, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Tampere (Finland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.