# Portesi Italian Foods, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/portesi-italian-foods-inc/9f7dedb5-6467-4987-9485-5766fe26a1f9

> Inspection records and compliance data for Portesi Italian Foods, Inc. in Stevens Point, Wisconsin. Access full analysis and detailed observations.

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## Details

- Name: Portesi Italian Foods, Inc.
- FEI Number: 3004154435
- City: Stevens Point
- State: Wisconsin
- Country Name: United States
- Address Line 1: 3201 Business Park Dr
- Zip Code: 54482

## Related Documents

- [FDA Inspection 1177885 - Portesi Italian Foods, Inc. - 2022-07-29](https://www.keypedia.com/records/fda_inspections/portesi-italian-foods-inc/b92fdb3b-f1d9-49ab-b0d7-8df02bd8a9b4) — classification: No Action Indicated (NAI), source: FDA, date: July 29, 2022
- [FDA Inspection 1062691 - Portesi Italian Foods, Inc. - 2018-07-26](https://www.keypedia.com/records/fda_inspections/portesi-italian-foods-inc/a43f6a3a-0019-49a1-ab66-f129627cfd6c) — classification: No Action Indicated (NAI), source: FDA, date: July 26, 2018
- [FDA Inspection 935168 - Portesi Italian Foods, Inc. - 2015-07-21](https://www.keypedia.com/records/fda_inspections/portesi-italian-foods-inc/85f27357-a162-4e97-bfa4-d0e489b873c9) — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2015
- [FDA Inspection 769353 - Portesi Italian Foods, Inc. - 2012-02-24](https://www.keypedia.com/records/fda_inspections/portesi-italian-foods-inc/0025a4b7-527c-4665-a0b1-f0a24f2124c4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 24, 2012
- [FDA Inspection 675064 - Portesi Italian Foods, Inc. - 2010-07-21](https://www.keypedia.com/records/fda_inspections/portesi-italian-foods-inc/2606d6e2-3e68-4b2f-bc13-2055d5060785) — classification: No Action Indicated (NAI), source: FDA, date: July 21, 2010
- [FDA Inspection 586581 - Portesi Italian Foods, Inc. - 2009-06-05](https://www.keypedia.com/records/fda_inspections/portesi-italian-foods-inc/fdd47e7e-5a82-4800-b973-dbeb1e302d20) — classification: No Action Indicated (NAI), source: FDA, date: June 5, 2009

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