# FDA Inspection 1282412 - Elos Medtech Timmersdala AB - August 21, 2025

Source: https://www.keypedia.com/records/fda_inspections/elos-medtech-timmersdala-ab/8483ef08-0cb1-4e22-943b-0fa807734c2f
Source feed: FDA_Inspections

> FDA Inspection 1282412 for Elos Medtech Timmersdala AB on August 21, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1282412
- Company Name: Elos Medtech Timmersdala AB
- Inspection Date: 2025-08-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices

## Related Documents

- [FDA Inspection 1282412 - 2025-08-21](https://www.keypedia.com/records/fda_inspections/elos-medtech-timmersdala-ab/6240d863-85de-46f7-bab2-4e08e64dc49b)
- [FDA Inspection 837222 - 2013-05-29](https://www.keypedia.com/records/fda_inspections/elos-medtech-timmersdala-ab/79c650d4-12de-473c-8252-0807cfb11f34)
- [FDA Inspection 698517 - 2010-10-14](https://www.keypedia.com/records/fda_inspections/elos-medtech-timmersdala-ab/ad9641a6-63f5-4e09-8c31-3c4a501156e9)

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