# FDA Inspection 1190646 - Elekta Inc - September 16, 2022

Source: https://www.keypedia.com/records/fda_inspections/elekta-inc/049d3289-e90f-46bc-ad9c-a67f0917a033
Source feed: FDA_Inspections

> FDA Inspection 1190646 for Elekta Inc on September 16, 2022. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1190646
- Company Name: Elekta Inc
- Inspection Date: 2022-09-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1190646 - 2022-09-16](https://www.keypedia.com/records/fda_inspections/elekta-inc/6908e35a-71dc-41a0-abff-fff90c127ba4)
- [FDA Inspection 1003704 - 2017-02-10](https://www.keypedia.com/records/fda_inspections/elekta-inc/549a27e2-daf8-456e-9e96-fc935b8a33f1)
- [FDA Inspection 1003704 - 2017-02-10](https://www.keypedia.com/records/fda_inspections/elekta-inc/e30dc953-f799-4178-a9b4-f8a3327e2101)
- [FDA Inspection 955076 - 2015-12-16](https://www.keypedia.com/records/fda_inspections/elekta-inc/c0cb219c-e48b-4579-a2b4-9dbf0cea99da)
- [FDA Inspection 955076 - 2015-12-16](https://www.keypedia.com/records/fda_inspections/elekta-inc/28f9d19e-4a9f-4041-a45a-ed7e3fcdcc29)

Company: https://www.keypedia.com/companies/elekta-inc/220c0a14-2bf9-4e56-9705-ccb709bd9a70

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