# Givaudan Flavors Corporation - Inspection Records

Source: https://www.keypedia.com/companies/givaudan-flavors-corporation/64351ff0-ac48-4cb3-8bd9-e429e780ecaf

> Inspection records and compliance data for Givaudan Flavors Corporation in Florence, Kentucky. Access full analysis and detailed observations.

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## Details

- Name: Givaudan Flavors Corporation
- FEI Number: 3000209926
- City: Florence
- State: Kentucky
- Country Name: United States
- Address Line 1: 9500 Sam Neace Dr
- Zip Code: 41042

## Related Documents

- [FDA Inspection 1156974 - Givaudan Flavors Corporation - 2021-11-04](https://www.keypedia.com/records/fda_inspections/givaudan-flavors-corporation/c05051ed-29e1-4b44-8cc3-e2cd5089500f) — classification: No Action Indicated (NAI), source: FDA, date: November 4, 2021
- [FDA Inspection 1035317 - Givaudan Flavors Corporation - 2017-11-15](https://www.keypedia.com/records/fda_inspections/givaudan-flavors-corporation/f15ed459-b57c-41f1-97a8-acb3e5162689) — classification: No Action Indicated (NAI), source: FDA, date: November 15, 2017
- [FDA Inspection 908156 - Givaudan Flavors Corporation - 2014-12-18](https://www.keypedia.com/records/fda_inspections/givaudan-flavors-corporation/9c030ca2-6e6e-4e13-95b1-d91022676e2a) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2014
- [FDA Inspection 908156 - Givaudan Flavors Corporation - 2014-12-18](https://www.keypedia.com/records/fda_inspections/givaudan-flavors-corporation/f801fd83-2494-414c-8e11-bd40de568f04) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2014
- [FDA Inspection 908156 - Givaudan Flavors Corporation - 2014-12-18](https://www.keypedia.com/records/fda_inspections/givaudan-flavors-corporation/5aafcaef-b1ea-45fa-be11-561d1e174ade) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2014
- [FDA Inspection 715907 - Givaudan Flavors Corporation - 2011-03-23](https://www.keypedia.com/records/fda_inspections/givaudan-flavors-corporation/32b6307a-50a8-4b72-8730-a8678e9038c2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 23, 2011

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