FDA Inspection 837222 — Elos Medtech Timmersdala AB
The FDA completed an inspection of Elos Medtech Timmersdala AB on May 29, 2013 in Timmersdala. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- May 29, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Timmersdala (Sweden)