# Publix Super Markets, Inc., Deerfield Beach, FL – FDA Inspections

Source: https://www.keypedia.com/companies/publix-super-markets-inc/39533f25-8a1e-45e0-8f9e-e2aadfb16650

> Inspection records and compliance data for Publix Super Markets, Inc. in Deerfield Beach, Florida. 6 FDA inspections on record, last inspected May 28, 2025.

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## Details

- Name: Publix Super Markets, Inc.
- FEI Number: 1051988
- Address Line 1: 777 Sw 12th Ave
- City: Deerfield Beach
- State: Florida
- Zip Code: 33442
- Country Name: United States
- Address: 777 Sw 12th Ave, Deerfield Beach, Florida 33442, United States
- Country: United States

## Related Documents

- FDA Inspection 1273050 - Publix Super Markets, Inc. - 2025-05-28 — source: FDA, date: May 28, 2025
- FDA Inspection 1252651 - Publix Super Markets, Inc. - 2024-07-09 — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2024
- FDA Inspection 1252651 - Publix Super Markets, Inc. - 2024-07-09 — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2024
- FDA Inspection 1252651 - Publix Super Markets, Inc. - 2024-07-09 — classification: No Action Indicated (NAI), source: FDA, date: July 9, 2024
- FDA Inspection 1207883 - Publix Super Markets, Inc. - 2023-05-31 — source: FDA, date: May 31, 2023
- FDA Inspection 1068979 - Publix Super Markets, Inc. - 2017-04-25 — classification: No Action Indicated (NAI), source: FDA, date: April 25, 2017
- [FDA Inspection 796046 - Publix Super Markets, Inc. - 2012-07-23](https://www.keypedia.com/records/fda_inspections/publix-super-markets-inc/d833e8a4-b132-43b6-be11-f5ef4c86feed) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 23, 2012
- FDA Inspection 576739 - Publix Super Markets, Inc. - 2009-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009
- FDA Inspection 576739 - Publix Super Markets, Inc. - 2009-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009
- FDA Inspection 576739 - Publix Super Markets, Inc. - 2009-04-15 — classification: No Action Indicated (NAI), source: FDA, date: April 15, 2009

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