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SUNSHINE PRODUCE LIMITED

⚠️ Moderate Risk

FEI: 3013308733 • TIANJIN • CHINA

FEI

FEI Number

3013308733

📍

Location

TIANJIN

🇨🇳

Country

CHINA
🏢

Address

5-2-101 TONGDASHANGCHEN, , TIANJIN, , China

Moderate Risk

FDA Import Risk Assessment

33.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
4/19/2017
Latest Refusal
4/19/2017
Earliest Refusal

Score Breakdown

Violation Severity
73.3×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

2381×

UNSAFE ADD

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.

38441×

SACCHARLBL

The article appears to contain Saccharin, a non-nutritive sweetener, and its label or labeling fails to list it as an added ingredient.

Refusal History

DateProductViolationsDivision
4/19/2017
20BGH10RAISINS, DRIED OR PASTE
11UNSAFE COL
238UNSAFE ADD
3844SACCHARLBL
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is SUNSHINE PRODUCE LIMITED's FDA import refusal history?

SUNSHINE PRODUCE LIMITED (FEI: 3013308733) has 1 FDA import refusal record(s) in our database, spanning from 4/19/2017 to 4/19/2017.

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. SUNSHINE PRODUCE LIMITED's FEI number is 3013308733.

What types of violations has SUNSHINE PRODUCE LIMITED received?

SUNSHINE PRODUCE LIMITED 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 SUNSHINE PRODUCE LIMITED come from?

All FDA import refusal data for SUNSHINE PRODUCE LIMITED 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.