# FDA Inspection 1123129 - Elekta, Inc. - December 13, 2019

Source: https://www.keypedia.com/records/fda_inspections/elekta-inc/5652bfd8-9731-4f82-a0cf-e60855a8b0c6
Source feed: FDA_Inspections

> FDA Inspection 1123129 for Elekta, Inc. on December 13, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1123129
- Company Name: Elekta, Inc.
- Inspection Date: 2019-12-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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Company: https://www.keypedia.com/companies/elekta-inc/19c772ce-d4b9-4cb7-bfa3-5f2fac4e2ba8

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