# Bama Sea Products,  Inc., St Petersburg, FL – FDA Inspections

Source: https://www.keypedia.com/companies/bama-sea-products-inc/eb296630-594c-4187-8c0e-f8d24685ce81

> Inspection records and compliance data for Bama Sea Products,  Inc. in St Petersburg, Florida. 7 FDA inspections on record, last inspected October 08, 2026.

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## Details

- Name: Bama Sea Products,  Inc.
- FEI Number: 1000114027
- Address Line 1: 756 28th St S
- City: St Petersburg
- State: Florida
- Zip Code: 33712
- Country Name: United States
- Address: 756 28th St S, St Petersburg, Florida 33712, United States
- Country: United States

## Related Documents

- FDA Inspection 1340898 - Bama Sea Products,  Inc. - 2026-10-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 8, 2026
- FDA Inspection 1237479 - Bama Sea Products,  Inc. - 2024-05-01 — source: FDA, date: May 1, 2024
- FDA Inspection 1002911 - Bama Sea Products,  Inc. - 2017-03-01 — source: FDA, date: March 1, 2017
- FDA Inspection 781068 - Bama Sea Products,  Inc. - 2012-05-10 — classification: No Action Indicated (NAI), source: FDA, date: May 10, 2012
- FDA Inspection 781068 - Bama Sea Products,  Inc. - 2012-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2012
- FDA Inspection 781068 - Bama Sea Products,  Inc. - 2012-05-10 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 10, 2012
- [FDA Inspection 678072 - Bama Sea Products,  Inc. - 2010-08-30](https://www.keypedia.com/records/fda_inspections/bama-sea-products-inc/d5001bbb-6259-4941-928f-b8e5abe2b286) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 30, 2010
- FDA Inspection 670439 - Bama Sea Products,  Inc. - 2010-06-30 — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2010
- [FDA Inspection 578705 - Bama Sea Products,  Inc. - 2009-04-24](https://www.keypedia.com/records/fda_inspections/bama-sea-products-inc/77a568f8-f335-4b7a-b4b8-d530c5f51197) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2009

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