# FDA Inspection 803107 - Icare Finland Oy - September 27, 2012

Source: https://www.keypedia.com/records/fda_inspections/icare-finland-oy/61e8a87a-fb41-46cc-a8bb-fec1c19965d9
Source feed: FDA_Inspections

> FDA Inspection 803107 for Icare Finland Oy on September 27, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803107
- Company Name: Icare Finland Oy
- Inspection Date: 2012-09-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 927346 - 2015-04-22](https://www.keypedia.com/records/fda_inspections/icare-finland-oy/51d535a8-a2f9-4561-a8dc-56fcc535f6d1)

Company: https://www.keypedia.com/companies/icare-finland-oy/c2676836-36a6-488b-b5f9-ff64abfec49c

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