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MULTIINVERSIONES A Y G

✅ Low Risk

FEI: 3017211532 • Guatemala • GUATEMALA

FEI

FEI Number

3017211532

📍

Location

Guatemala

🇬🇹

Country

GUATEMALA
🏢

Address

Calle 150 Colonia Belen, , Guatemala, , Guatemala

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
9/15/2020
Latest Refusal
9/15/2020
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

Refusal History

DateProductViolationsDivision
9/15/2020
80QKRFACE MASK (EXCEPT N95 RESPIRATOR) FOR GENERAL PUBLIC/HEALTHCARE PERSONNEL PER IIE GUIDANCE
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is MULTIINVERSIONES A Y G's FDA import refusal history?

MULTIINVERSIONES A Y G (FEI: 3017211532) has 1 FDA import refusal record(s) in our database, spanning from 9/15/2020 to 9/15/2020.

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. MULTIINVERSIONES A Y G's FEI number is 3017211532.

What types of violations has MULTIINVERSIONES A Y G received?

MULTIINVERSIONES A Y G has been cited for 1 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 MULTIINVERSIONES A Y G come from?

All FDA import refusal data for MULTIINVERSIONES A Y G 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.