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AURANDINA SAC

⚠️ Moderate Risk

FEI: 3015218528 • Lima, PE-LIM • PERU

FEI

FEI Number

3015218528

📍

Location

Lima, PE-LIM

🇵🇪

Country

PERU
🏢

Address

Calle 3 Mz M Lote 1e Villa El Salvador, , Lima, PE-LIM, Peru

Moderate Risk

FDA Import Risk Assessment

31.0
LowModerateHighCritical

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

Statistics

7
Total Refusals
2
Unique Violations
7/10/2013
Latest Refusal
7/10/2013
Earliest Refusal

Score Breakdown

Violation Severity
35.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

3247×

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)).

3287×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
7/10/2013
31LFT30TEA, INSTANT, PLAIN, DECAFFEINATED
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)
7/10/2013
31LFT30TEA, INSTANT, PLAIN, DECAFFEINATED
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)
7/10/2013
31LFT30TEA, INSTANT, PLAIN, DECAFFEINATED
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)
7/10/2013
31LFT02TEA, GREEN, DECAFFEINATED
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)
7/10/2013
31LFT06TEA, SCENTED, DECAFFEINATED
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)
7/10/2013
31PFT04TEA, CAMOMILLE, CHAMOMILE (TEA SUBSTITUTE)
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)
7/10/2013
31PFT06TEA, ROSE HIP (TEA SUBSTITUTE)
324NO ENGLISH
328USUAL NAME
Florida District Office (FLA-DO)

Frequently Asked Questions

What is AURANDINA SAC's FDA import refusal history?

AURANDINA SAC (FEI: 3015218528) has 7 FDA import refusal record(s) in our database, spanning from 7/10/2013 to 7/10/2013.

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. AURANDINA SAC's FEI number is 3015218528.

What types of violations has AURANDINA SAC received?

AURANDINA SAC has been cited for 2 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 AURANDINA SAC come from?

All FDA import refusal data for AURANDINA SAC 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.