# Elekta Inc – FDA Inspection, Feb 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/elekta-inc/e30dc953-f799-4178-a9b4-f8a3327e2101
Source feed: FDA_Inspections

> FDA inspection 1003704 of Elekta Inc, February 10, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003704
- Company Name: Elekta Inc
- Inspection Date: 2017-02-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: 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 955076 - 2015-12-16
- [FDA Inspection 730299 - 2011-06-17](https://www.keypedia.com/records/fda_inspections/elekta-inc/4b1e5f02-757a-466f-bbbd-007be20107aa)
- FDA Inspection 665312 - 2010-05-14

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)
- [FDA Associated Person](https://www.keypedia.com/people/eric-m-padgett/a42150bc-aa7f-4076-8a68-af47ff465bac)

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