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Siang Cung Mang Thangnget

✅ Low Risk

FEI: 3011106305 • Yangon, Yangon • MYANMAR

FEI

FEI Number

3011106305

📍

Location

Yangon, Yangon

🇲🇲

Country

MYANMAR
🏢

Address

6-B 245 Bo Myat Tun Street Rm, , Yangon, Yangon, Myanmar

Low Risk

FDA Import Risk Assessment

22.7
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

3
Total Refusals
3
Unique Violations
12/12/2014
Latest Refusal
12/12/2014
Earliest Refusal

Score Breakdown

Violation Severity
32.5×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

3242×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

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.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
12/12/2014
02DGT99RICE, PROCESSED (PACKAGED) N.E.C.
324NO ENGLISH
Detroit District Office (DET-DO)
12/12/2014
38CFH28MIXED VEGETABLE SOUP, DRIED
324NO ENGLISH
Detroit District Office (DET-DO)
12/12/2014
04CFH99NOODLES AND NOODLE PRODUCTS, N.E.C.
321LACKS N/C
482NUTRIT LBL
Detroit District Office (DET-DO)

Frequently Asked Questions

What is Siang Cung Mang Thangnget's FDA import refusal history?

Siang Cung Mang Thangnget (FEI: 3011106305) has 3 FDA import refusal record(s) in our database, spanning from 12/12/2014 to 12/12/2014.

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. Siang Cung Mang Thangnget's FEI number is 3011106305.

What types of violations has Siang Cung Mang Thangnget received?

Siang Cung Mang Thangnget 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 Siang Cung Mang Thangnget come from?

All FDA import refusal data for Siang Cung Mang Thangnget 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.