# Leventon S. A. U. – FDA Inspection, Mar 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/leventon-s-a-u/a8c6339a-a163-4f66-86fd-df81aa6b299e
Source feed: FDA_Inspections

> FDA inspection 1046509 of Leventon S. A. U., March 22, 2018. Classification: Official Action Indicated (OAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1046509
- Company Name: Leventon S. A. U.
- Inspection Date: 2018-03-22
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- FDA Inspection 945390 - 2015-09-24
- [FDA Inspection 716215 - 2011-02-24](https://www.keypedia.com/records/fda_inspections/leventon-s-a-u/cda85ee8-b6cf-4b09-ac47-42db9351972f)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

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