# EDAP - TMS  France SA – FDA Inspection, Mar 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/edap-tms-france-sa/a2353e40-7ef2-46b2-b98d-297291c903cf
Source feed: FDA_Inspections

> FDA inspection 1047540 of EDAP - TMS  France SA, March 22, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047540
- Company Name: EDAP - TMS  France SA
- Inspection Date: 2018-03-22
- 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: 1

## Related Documents

- FDA Inspection 810862 - 2012-12-13

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/james-a-lane/f6cd3d8d-7de9-45c5-9380-7e0c5de4720e)

Company: https://www.keypedia.com/companies/edap-tms-france-sa/4251d620-ccd4-4a96-a97b-aecd4edbafc4

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