# PFG Specialty, Inc. DBA Bar Harbor Seafood, Orlando, FL – FDA Inspections

Source: https://www.keypedia.com/companies/pfg-specialty-inc-dba-bar-harbor-seafood/d7bd70f0-3594-4dfb-97a6-08fdc21c8739

> Inspection records and compliance data for PFG Specialty, Inc. DBA Bar Harbor Seafood in Orlando, Florida. 5 FDA inspections on record, 1 Form 483, last inspected April 18, 2025.

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## Details

- Name: PFG Specialty, Inc. DBA Bar Harbor Seafood
- FEI Number: 1000113811
- Address Line 1: 2000 Premier Row
- City: Orlando
- State: Florida
- Zip Code: 32809
- Country Name: United States
- Address: 2000 Premier Row, Orlando, Florida 32809, United States
- Country: United States

## Related Documents

- [FDA Inspection 1267225 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2025-04-18](https://www.keypedia.com/records/fda_inspections/pfg-specialty-inc-dba-bar-harbor-seafood/5a54b519-5fcc-40b3-870a-435ea855f9a6) — source: FDA, date: April 18, 2025
- FDA Inspection 1089181 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2019-05-03 — source: FDA, date: May 3, 2019
- [FDA Inspection 781003 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2012-05-10](https://www.keypedia.com/records/fda_inspections/pfg-specialty-inc-dba-bar-harbor-seafood/57fdbe83-ba2b-43f3-86b9-91e09e0d1914) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2012
- FDA Inspection 663364 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2010-05-28 — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2010
- FDA Inspection 663364 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2010-05-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 28, 2010
- FDA Inspection 663364 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2010-05-28 — classification: No Action Indicated (NAI), source: FDA, date: May 28, 2010
- [FDA Inspection 567922 - PFG Specialty, Inc. DBA Bar Harbor Seafood - 2009-03-04](https://www.keypedia.com/records/fda_inspections/pfg-specialty-inc-dba-bar-harbor-seafood/7dc202ee-96f6-4319-a000-2740c3bad649) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2009

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