# Elekta, Inc. – FDA Inspection, Nov 21, 2011

Source: https://www.keypedia.com/records/fda_inspections/elekta-inc/4b3b104d-bae3-4511-b7db-9bd084eebf41
Source feed: FDA_Inspections

> FDA inspection 753194 of Elekta, Inc., November 21, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 753194
- Company Name: Elekta, Inc.
- Inspection Date: 2011-11-21
- 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: 1

## Related Documents

- FDA Inspection 940239 - 2015-08-26
- FDA Inspection 616125 - 2009-09-28

Company: https://www.keypedia.com/companies/elekta-inc/4dd144dc-7caa-42d9-bb35-f4f60970a67e

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