# FDA Inspection 1002026 - RAUMEDIC Estonia AS - January 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/raumedic-estonia-as/39336474-027c-4643-8367-225d8345b7c4
Source feed: FDA_Inspections

> FDA Inspection 1002026 for RAUMEDIC Estonia AS on January 26, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1002026
- Company Name: RAUMEDIC Estonia AS
- Inspection Date: 2017-01-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 819197 - 2013-01-29](https://www.keypedia.com/records/fda_inspections/raumedic-estonia-as/4c6c2ea6-58d5-4af0-b418-d77d9448de0c)

Company: https://www.keypedia.com/companies/raumedic-estonia-as/c2842f1a-fb45-46e5-9063-6670c0c397f0

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