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Geyer Freres

⚠️ Moderate Risk

FEI: 3004010550 • Munster • FRANCE

FEI

FEI Number

3004010550

📍

Location

Munster

🇫🇷

Country

FRANCE
🏢

Address

Rue De Torcheville 57670, , Munster, , France

Moderate Risk

FDA Import Risk Assessment

27.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
12/14/2004
Latest Refusal
12/14/2004
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
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.

4882×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

Refusal History

DateProductViolationsDivision
12/14/2004
29BCT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
482NUTRIT LBL
488HEALTH C
Baltimore District Office (BLT-DO)
12/14/2004
29BCT02SOFT DRINK, CITRUS FRUIT FLAVORED, CARBONATED
482NUTRIT LBL
488HEALTH C
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Geyer Freres's FDA import refusal history?

Geyer Freres (FEI: 3004010550) has 2 FDA import refusal record(s) in our database, spanning from 12/14/2004 to 12/14/2004.

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. Geyer Freres's FEI number is 3004010550.

What types of violations has Geyer Freres received?

Geyer Freres 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 Geyer Freres come from?

All FDA import refusal data for Geyer Freres 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.