# Integra NeuroSciences Implants (France) S.A.S., Sophia Antipolis Cedex, France – FDA Inspections

Source: https://www.keypedia.com/companies/integra-neurosciences-implants-france-sas/8a4a43ac-745b-4afc-804b-fe7cfc6acbdb

> Inspection records and compliance data for Integra NeuroSciences Implants (France) S.A.S. in Sophia Antipolis Cedex. 4 FDA inspections on record, 2 Form 483s, last inspected October 30, 2018.

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## Details

- Name: Integra NeuroSciences Implants (France) S.A.S.
- FEI Number: 3003813779
- Address Line 1: Integra Neurosciences, 2905 Route Des Dolines; Valbonne
- City: Sophia Antipolis Cedex
- Country Name: France
- Address: Integra Neurosciences, 2905 Route Des Dolines; Valbonne, Sophia Antipolis Cedex, France
- Country: France

## Related Documents

- [FDA Inspection 1124076 - Integra NeuroSciences Implants (France) S.A.S. - 2018-10-30](https://www.keypedia.com/records/fda_inspections/integra-neurosciences-implants-france-sas/e6ec95e7-0e9f-4edb-aaab-1bf62d690efe) — source: FDA, date: October 30, 2018
- [FDA Inspection 1107850 - Integra NeuroSciences Implants (France) S.A.S. - 2018-09-06](https://www.keypedia.com/records/fda_inspections/integra-neurosciences-implants-france-sas/ed10c3de-f1a1-4a5f-b02b-977f7bb304ef) — source: FDA, date: September 6, 2018
- FDA Inspection 914092 - Integra NeuroSciences Implants (France) S.A.S. - 2015-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2015
- [FDA Inspection 914092 - Integra NeuroSciences Implants (France) S.A.S. - 2015-02-12](https://www.keypedia.com/records/fda_inspections/integra-neurosciences-implants-france-sas/36d41a71-0b06-48b1-885f-d3015a831393) — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2015
- FDA Inspection 555074 - Integra NeuroSciences Implants (France) S.A.S. - 2008-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2008
- FDA Inspection 555074 - Integra NeuroSciences Implants (France) S.A.S. - 2008-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2008

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