# Elekta Inc – FDA Inspection, Jun 17, 2011

Source: https://www.keypedia.com/records/fda_inspections/elekta-inc/4b1e5f02-757a-466f-bbbd-007be20107aa
Source feed: FDA_Inspections

> FDA inspection 730299 of Elekta Inc, June 17, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 730299
- Company Name: Elekta Inc
- Inspection Date: 2011-06-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1190646 - 2022-09-16
- [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
- FDA Inspection 665312 - 2010-05-14

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