# FDA Inspection 1044275 - Teoxane S.A. - June 29, 2017

Source: https://www.keypedia.com/records/fda_inspections/teoxane-sa/b705597c-bb9b-4054-b72d-697f820acd11
Source feed: FDA_Inspections

> FDA Inspection 1044275 for Teoxane S.A. on June 29, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1044275
- Company Name: Teoxane S.A.
- Inspection Date: 2017-06-29
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 806598 - 2012-11-16](https://www.keypedia.com/records/fda_inspections/teoxane-sa/0d041736-d063-41e6-ae57-7d5ad3d801c4)

Company: https://www.keypedia.com/companies/teoxane-sa/fea686af-63ac-4110-aef8-5ef7eaa5b2e4

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