# Icare Finland Oy – FDA Inspection, Sep 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 of Icare Finland Oy, September 27, 2012. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- 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: 5

## Related Documents

- [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