# Leventon S. A. U. – FDA Inspection, Feb 24, 2011

Source: https://www.keypedia.com/records/fda_inspections/leventon-s-a-u/cda85ee8-b6cf-4b09-ac47-42db9351972f
Source feed: FDA_Inspections

> FDA inspection 716215 of Leventon S. A. U., February 24, 2011. Classification: Voluntary Action Indicated (VAI). 4 citations 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: 716215
- Company Name: Leventon S. A. U.
- Inspection Date: 2011-02-24
- 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: 4

## Related Documents

- [FDA Inspection 1046509 - 2018-03-22](https://www.keypedia.com/records/fda_inspections/leventon-s-a-u/a8c6339a-a163-4f66-86fd-df81aa6b299e)
- FDA Inspection 945390 - 2015-09-24

Company: https://www.keypedia.com/companies/leventon-s-a-u/524a4a3e-36d6-4e4f-b6c8-59b577f87b00

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