# RAUMEDIC Estonia AS – FDA Inspection, Jan 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 of RAUMEDIC Estonia AS, January 26, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 2

## Related Documents

- FDA Inspection 819197 - 2013-01-29

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

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