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Embotelladora India Quinche

✅ Low Risk

FEI: 3009085145 • El Quinche • GUATEMALA

FEI

FEI Number

3009085145

📍

Location

El Quinche

🇬🇹

Country

GUATEMALA
🏢

Address

7 Av. 7-31 Zona 5santa Cruz Del Quinche, , El Quinche, , Guatemala

Low Risk

FDA Import Risk Assessment

23.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
1
Unique Violations
11/8/2012
Latest Refusal
11/8/2012
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

4822×

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
11/8/2012
29BGT07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, CARBONATED
482NUTRIT LBL
Division of Southeast Imports (DSEI)
11/8/2012
29BGT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Embotelladora India Quinche's FDA import refusal history?

Embotelladora India Quinche (FEI: 3009085145) has 2 FDA import refusal record(s) in our database, spanning from 11/8/2012 to 11/8/2012.

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. Embotelladora India Quinche's FEI number is 3009085145.

What types of violations has Embotelladora India Quinche received?

Embotelladora India Quinche 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 Embotelladora India Quinche come from?

All FDA import refusal data for Embotelladora India Quinche 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.