# Rhino Foods, Inc., Burlington, VT – FDA Inspections

Source: https://www.keypedia.com/companies/rhino-foods-inc/c0d9d709-a22d-40a2-ab28-141bd7fb6d99

> Inspection records and compliance data for Rhino Foods, Inc. in Burlington, Vermont. 8 FDA inspections on record, 1 Form 483, last inspected May 06, 2026.

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## Details

- Name: Rhino Foods, Inc.
- FEI Number: 1000513547
- Address Line 1: 179 Queen City Park Rd
- City: Burlington
- State: Vermont
- Zip Code: 05401
- Country Name: United States
- Address: 179 Queen City Park Rd, Burlington, Vermont 05401, United States
- Country: United States

## Related Documents

- FDA Inspection 1288429 - Rhino Foods, Inc. - 2026-05-06 — source: FDA, date: May 6, 2026
- FDA Inspection 1230549 - Rhino Foods, Inc. - 2024-02-08 — source: FDA, date: February 8, 2024
- [FDA Inspection 1135910 - Rhino Foods, Inc. - 2021-02-22](https://www.keypedia.com/records/fda_inspections/rhino-foods-inc/6116fb28-b68f-42b8-b4a0-9af51582c8b8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 22, 2021
- FDA Inspection 1129697 - Rhino Foods, Inc. - 2020-08-25 — classification: No Action Indicated (NAI), source: FDA, date: August 25, 2020
- [FDA Inspection 1015501 - Rhino Foods, Inc. - 2017-06-21](https://www.keypedia.com/records/fda_inspections/rhino-foods-inc/6635ffc3-a0a5-4c78-b5fb-dbe2b79af327) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 21, 2017
- FDA Inspection 866267 - Rhino Foods, Inc. - 2014-02-11 — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2014
- FDA Inspection 766157 - Rhino Foods, Inc. - 2012-02-02 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 2, 2012
- [FDA Inspection 766157 - Rhino Foods, Inc. - 2012-02-02](https://www.keypedia.com/records/fda_inspections/rhino-foods-inc/f2aa01ab-47b5-48b6-b71b-87dfaa7244d1) — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2012
- FDA Inspection 605370 - Rhino Foods, Inc. - 2009-08-05 — classification: No Action Indicated (NAI), source: FDA, date: August 5, 2009

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