# FDA Inspection 698517 - Elos Medtech Timmersdala AB - October 14, 2010

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-timmersdala-ab/ad9641a6-63f5-4e09-8c31-3c4a501156e9
Source feed: FDA_Inspections

> FDA Inspection 698517 for Elos Medtech Timmersdala AB on October 14, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 698517
- Company Name: Elos Medtech Timmersdala AB
- Inspection Date: 2010-10-14
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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