# Golden Eye Seafood, LLC, Tall Timbers, MD – FDA Inspections

Source: https://www.keypedia.com/companies/golden-eye-seafood-llc/207a7d5d-c24a-4e07-8630-adb4590ea5ea

> Inspection records and compliance data for Golden Eye Seafood, LLC in Tall Timbers, Maryland. 5 FDA inspections on record, 2 Form 483s, last inspected July 11, 2025.

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## Details

- Name: Golden Eye Seafood, LLC
- FEI Number: 3002609056
- Address Line 1: 17640 Clarke Rd
- City: Tall Timbers
- State: Maryland
- Zip Code: 20690
- Country Name: United States
- Address: 17640 Clarke Rd, Tall Timbers, Maryland 20690, United States
- Country: United States

## Related Documents

- FDA Inspection 1275501 - Golden Eye Seafood, LLC - 2025-07-11 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 11, 2025
- [FDA Inspection 1275501 - Golden Eye Seafood, LLC - 2025-07-11](https://www.keypedia.com/records/fda_inspections/golden-eye-seafood-llc/11ee1302-748e-4243-a1c6-bab5576fe4d8) — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- FDA Inspection 1275501 - Golden Eye Seafood, LLC - 2025-07-11 — classification: No Action Indicated (NAI), source: FDA, date: July 11, 2025
- [FDA Inspection 1148620 - Golden Eye Seafood, LLC - 2021-08-11](https://www.keypedia.com/records/fda_inspections/golden-eye-seafood-llc/ab4fa178-9816-49a6-9120-237ba5a8772b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 11, 2021
- [FDA Inspection 1031450 - Golden Eye Seafood, LLC - 2017-11-15](https://www.keypedia.com/records/fda_inspections/golden-eye-seafood-llc/750ce5c1-d99a-4de4-9e3c-abfd7b692dc5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2017
- [FDA Inspection 855869 - Golden Eye Seafood, LLC - 2013-11-20](https://www.keypedia.com/records/fda_inspections/golden-eye-seafood-llc/87808de1-04fd-4551-9b4f-18331d5c43d2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2013
- FDA Inspection 802975 - Golden Eye Seafood, LLC - 2012-10-12 — classification: No Action Indicated (NAI), source: FDA, date: October 12, 2012

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