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Abbott Products GmbH

⚠️ Moderate Risk

FEI: 3000275148 • Hanover, Lower Saxony • GERMANY

FEI

FEI Number

3000275148

📍

Location

Hanover, Lower Saxony

🇩🇪

Country

GERMANY
🏢

Address

Hans-bockler-allee 20, , Hanover, Lower Saxony, Germany

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/22/2004
Latest Refusal
7/22/2004
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

3063×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

Refusal History

DateProductViolationsDivision
7/22/2004
02HYY99STARCH PRODUCTS N.E.C.
306INSANITARY
Cincinnati District Office (CIN-DO)
7/22/2004
09CYY33CASEINATES
306INSANITARY
Cincinnati District Office (CIN-DO)
7/22/2004
26CYY04OLIVE OIL, REFINED, SINGLE INGREDIENT
306INSANITARY
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Abbott Products GmbH's FDA import refusal history?

Abbott Products GmbH (FEI: 3000275148) has 3 FDA import refusal record(s) in our database, spanning from 7/22/2004 to 7/22/2004.

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. Abbott Products GmbH's FEI number is 3000275148.

What types of violations has Abbott Products GmbH received?

Abbott Products GmbH 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 Abbott Products GmbH come from?

All FDA import refusal data for Abbott Products GmbH 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.