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RIVIS

⚠️ Moderate Risk

FEI: 3009790459 • Agua Prieta, Sonora • MEXICO

FEI

FEI Number

3009790459

📍

Location

Agua Prieta, Sonora

🇲🇽

Country

MEXICO
🏢

Address

Calle 18 No. 2340, Col. Vallarta, Agua Prieta, Agua Prieta, Sonora, Mexico

Moderate Risk

FDA Import Risk Assessment

30.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
2
Unique Violations
12/7/2012
Latest Refusal
12/7/2012
Earliest Refusal

Score Breakdown

Violation Severity
65.0×40%
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

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.

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

Refusal History

DateProductViolationsDivision
12/7/2012
28LHT99MIXED SPICES AND SEASONINGS, LIQUID, WITH SALT, N.E.C.
482NUTRIT LBL
75UNAPPROVED
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is RIVIS's FDA import refusal history?

RIVIS (FEI: 3009790459) has 1 FDA import refusal record(s) in our database, spanning from 12/7/2012 to 12/7/2012.

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. RIVIS's FEI number is 3009790459.

What types of violations has RIVIS received?

RIVIS 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 RIVIS come from?

All FDA import refusal data for RIVIS 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.