# BRETT ANTHONY FOODS, Northbrook, IL – FDA Inspections

Source: https://www.keypedia.com/companies/brett-anthony-foods/4ec5b2a8-bcb0-4f64-924f-7389c1e68b12

> Inspection records and compliance data for BRETT ANTHONY FOODS in Northbrook, Illinois. 8 FDA inspections on record, last inspected February 27, 2026.

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## Details

- Name: BRETT ANTHONY FOODS
- FEI Number: 3001751233
- Address Line 1: 1921 Raymond Dr
- City: Northbrook
- State: Illinois
- Zip Code: 60062
- Country Name: United States
- Address: 1921 Raymond Dr, Northbrook, Illinois 60062, United States
- Country: United States

## Related Documents

- FDA Inspection 1286501 - BRETT ANTHONY FOODS - 2026-02-27 — source: FDA, date: February 27, 2026
- FDA Inspection 1195493 - BRETT ANTHONY FOODS - 2023-01-13 — source: FDA, date: January 13, 2023
- FDA Inspection 1069973 - BRETT ANTHONY FOODS - 2018-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2018
- FDA Inspection 1069973 - BRETT ANTHONY FOODS - 2018-09-24 — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2018
- FDA Inspection 963373 - BRETT ANTHONY FOODS - 2015-12-15 — classification: No Action Indicated (NAI), source: FDA, date: December 15, 2015
- [FDA Inspection 772515 - BRETT ANTHONY FOODS - 2012-04-10](https://www.keypedia.com/records/fda_inspections/brett-anthony-foods/0b116cc5-a60e-4224-8e5b-a941ce81908b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2012
- [FDA Inspection 717857 - BRETT ANTHONY FOODS - 2011-04-04](https://www.keypedia.com/records/fda_inspections/brett-anthony-foods/5b545a78-73df-4726-8b78-c96a3cbb3907) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 4, 2011
- [FDA Inspection 651800 - BRETT ANTHONY FOODS - 2010-03-11](https://www.keypedia.com/records/fda_inspections/brett-anthony-foods/9dbb8b0a-ec98-4429-b572-d2857275f4cc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 11, 2010
- FDA Inspection 608050 - BRETT ANTHONY FOODS - 2009-08-19 — classification: No Action Indicated (NAI), source: FDA, date: August 19, 2009

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