# Lanovara Specialty Foods, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/lanovara-specialty-foods-inc/08c7fa3e-35dd-4c85-9194-e666c88fea63

> Inspection records and compliance data for Lanovara Specialty Foods, Inc. in Rochester, New York. Access full analysis and detailed observations.

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## Details

- Name: Lanovara Specialty Foods, Inc.
- FEI Number: 1381489
- City: Rochester
- State: New York
- Country Name: United States
- Address Line 1: 208 Mushroom Blvd
- Zip Code: 14623

## Related Documents

- [FDA Inspection 1269242 - Lanovara Specialty Foods, Inc. - 2025-04-23](https://www.keypedia.com/records/fda_inspections/lanovara-specialty-foods-inc/45604539-8bc3-4066-b3f7-ba5b8aee104b) — source: FDA, date: April 23, 2025
- [FDA Inspection 1181818 - Lanovara Specialty Foods, Inc. - 2022-10-20](https://www.keypedia.com/records/fda_inspections/lanovara-specialty-foods-inc/8268a9cb-4053-4d72-be8d-6c01e075124e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 20, 2022
- [FDA Inspection 999207 - Lanovara Specialty Foods, Inc. - 2017-01-27](https://www.keypedia.com/records/fda_inspections/lanovara-specialty-foods-inc/1843e5f6-fd7b-4c0e-a8f9-6e47768c9ce3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 27, 2017
- [FDA Inspection 858465 - Lanovara Specialty Foods, Inc. - 2013-12-11](https://www.keypedia.com/records/fda_inspections/lanovara-specialty-foods-inc/fd32c74f-5c9e-4e17-95d4-add65cd8018b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 11, 2013
- [FDA Inspection 685770 - Lanovara Specialty Foods, Inc. - 2010-10-14](https://www.keypedia.com/records/fda_inspections/lanovara-specialty-foods-inc/e24a563e-1a70-4ee2-8b66-6d421d40deb5) — classification: No Action Indicated (NAI), source: FDA, date: October 14, 2010
- [FDA Inspection 685770 - Lanovara Specialty Foods, Inc. - 2010-10-14](https://www.keypedia.com/records/fda_inspections/lanovara-specialty-foods-inc/89624080-832d-42b0-bbeb-affb35e5f9b6) — classification: No Action Indicated (NAI), source: FDA, date: October 14, 2010

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