# FDA Inspection 680394 - Elekta Limited - September 29, 2010

Source: https://www.keypedia.com/records/fda_inspections/elekta-limited/61b3a94a-ab2b-49e4-ae32-b3d98c28dac4
Source feed: FDA_Inspections

> FDA Inspection 680394 for Elekta Limited on September 29, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 680394
- Company Name: Elekta Limited
- Inspection Date: 2010-09-29
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/elekta-limited/0f556633-ae04-46a4-9a30-69f63809b752

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