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GOLDEN SEA COLD STORE AND PROCESSING PLANT

⚠️ Moderate Risk

FEI: 3017087274 • Yangon

FEI

FEI Number

3017087274

📍

Location

Yangon

🌍

Country

🏢

Address

No. 3 D1, Twin Thin Taik Wun U Tun, Nyo Street, Industrial Zone, Yangon, ,

Moderate Risk

FDA Import Risk Assessment

27.1
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

1
Total Refusals
3
Unique Violations
5/17/2021
Latest Refusal
5/17/2021
Earliest Refusal

Score Breakdown

Violation Severity
53.3×40%
Refusal Volume
11.2×30%
Recency
6.9×20%
Frequency
10.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3211×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

37011×

ALRGN402A4

it appears to be adulterated within the meaning of section 402(a)(4) because it appears that the food was prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health, specifically because the food appears to contain a major food allergen through insanitary conditions that led to cross-contact.

Refusal History

DateProductViolationsDivision
5/17/2021
16AVD09CARP
218LIST INGRE
321LACKS N/C
3701ALRGN402A4
Division of Northeast Imports (DNEI)

Frequently Asked Questions

What is GOLDEN SEA COLD STORE AND PROCESSING PLANT's FDA import refusal history?

GOLDEN SEA COLD STORE AND PROCESSING PLANT (FEI: 3017087274) has 1 FDA import refusal record(s) in our database, spanning from 5/17/2021 to 5/17/2021.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. GOLDEN SEA COLD STORE AND PROCESSING PLANT's FEI number is 3017087274.

What types of violations has GOLDEN SEA COLD STORE AND PROCESSING PLANT received?

GOLDEN SEA COLD STORE AND PROCESSING PLANT has been cited for 3 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about GOLDEN SEA COLD STORE AND PROCESSING PLANT come from?

All FDA import refusal data for GOLDEN SEA COLD STORE AND PROCESSING PLANT is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.