# Elos Medtech Timmersdala AB – FDA Inspection, Oct 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 of Elos Medtech Timmersdala AB, October 14, 2010. Classification: Official Action Indicated (OAI). 6 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 1282412 - 2025-08-21
- FDA Inspection 837222 - 2013-05-29

Company: https://www.keypedia.com/companies/elos-medtech-timmersdala-ab/0fc59f5a-6d36-43d8-b3ab-834fcaffaf36

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