Brijon Limited
FDA import alert and refusal historyPort-Of-Spain, Trinidad and TobagoFEI 3011977155
Recorded by FDA as BRIJON LIMITED
As of October 26, 2026, Brijon Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 19, 2018, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Snapper (red, gray, malabar, etc.) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Brijon Limited
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Brijon Limited
- Is Brijon Limited on an FDA import alert?
- No listing for Brijon Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Trinidad and Tobago page.
- Has FDA refused shipments from Brijon Limited?
- Yes. FDA refused 1 shipment line from Brijon Limited on September 19, 2018. The most recent, on September 19, 2018, was snapper (red, gray, malabar, etc.), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Brijon Limited's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Brijon Limited's FEI number?
- Brijon Limited's FDA Establishment Identifier (FEI) is 3011977155.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.