# Southcoast Fish Company of Broward, LLC, Pompano Beach, FL – FDA Inspections

Source: https://www.keypedia.com/companies/southcoast-fish-company-of-broward-llc/cda0005a-6b4d-4282-bfb0-264ad825032c

> Inspection records and compliance data for Southcoast Fish Company of Broward, LLC in Pompano Beach, Florida. 5 FDA inspections on record, 2 Form 483s, last inspected December 22, 2025.

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## Details

- Name: Southcoast Fish Company of Broward, LLC
- FEI Number: 3001452847
- Address Line 1: 999 S Dixie Hwy W
- City: Pompano Beach
- State: Florida
- Zip Code: 33060
- Country Name: United States
- Address: 999 S Dixie Hwy W, Pompano Beach, Florida 33060, United States
- Country: United States

## Related Documents

- [FDA Inspection 1283681 - Southcoast Fish Company of Broward, LLC - 2025-12-22](https://www.keypedia.com/records/fda_inspections/southcoast-fish-company-of-broward-llc/2a676ba3-3d87-4a89-94d2-fe68af4120c2) — source: FDA, date: December 22, 2025
- [FDA Inspection 1197554 - Southcoast Fish Company of Broward, LLC - 2023-02-07](https://www.keypedia.com/records/fda_inspections/southcoast-fish-company-of-broward-llc/ead26c87-5125-42eb-b4f7-7b43f7d54124) — source: FDA, date: February 7, 2023
- FDA Inspection 992851 - Southcoast Fish Company of Broward, LLC - 2016-10-27 — source: FDA, date: October 27, 2016
- [FDA Inspection 706052 - Southcoast Fish Company of Broward, LLC - 2011-01-13](https://www.keypedia.com/records/fda_inspections/southcoast-fish-company-of-broward-llc/f64ba10c-c392-4633-9456-f116183e3f0e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 13, 2011
- FDA Inspection 695920 - Southcoast Fish Company of Broward, LLC - 2010-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2010
- FDA Inspection 695920 - Southcoast Fish Company of Broward, LLC - 2010-10-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 21, 2010
- FDA Inspection 695920 - Southcoast Fish Company of Broward, LLC - 2010-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2010

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