# Inion Oy – FDA Inspection, Nov 15, 2022

Source: https://www.keypedia.com/records/fda_inspections/inion-oy/1f3d062f-6581-4d36-be11-5249890532fc
Source feed: FDA_Inspections

> FDA inspection 1190792 of Inion Oy, November 15, 2022. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1190792
- Company Name: Inion Oy
- Inspection Date: 2022-11-15
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1276424 - 2025-06-03
- FDA Inspection 841653 - 2013-06-20
- [FDA Inspection 710111 - 2011-02-10](https://www.keypedia.com/records/fda_inspections/inion-oy/9fc686d7-21db-49dc-9779-457244f68aee)

Company: https://www.keypedia.com/companies/inion-oy/4e9f14f3-87f1-4888-bac0-756a59c3713f

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7