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Schweizer-Effax Gmbh

⚠️ High Risk

FEI: 3004008582 • Nordwalde, North Rhine-Westphalia • GERMANY

FEI

FEI Number

3004008582

📍

Location

Nordwalde, North Rhine-Westphalia

🇩🇪

Country

GERMANY
🏢

Address

Westring 24, , Nordwalde, North Rhine-Westphalia, Germany

High Risk

FDA Import Risk Assessment

51.6
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

10
Total Refusals
3
Unique Violations
5/11/2011
Latest Refusal
9/9/2010
Earliest Refusal

Score Breakdown

Violation Severity
75.0×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

727×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

1182×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

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
5/11/2011
64APL99DISINFECTANT N.E.C.
75UNAPPROVED
Southwest Import District Office (SWI-DO)
2/14/2011
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Southwest Import District Office (SWI-DO)
10/27/2010
66PBJ99ULTRAVIOLET SCREEN/SUNSCREEN N.E.C.
118NOT LISTED
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)
9/9/2010
68YAO99OTHER ANIMAL, N.E.C. ANIMAL DRUGS N.E.C.
72NEW VET DR
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Schweizer-Effax Gmbh's FDA import refusal history?

Schweizer-Effax Gmbh (FEI: 3004008582) has 10 FDA import refusal record(s) in our database, spanning from 9/9/2010 to 5/11/2011.

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. Schweizer-Effax Gmbh's FEI number is 3004008582.

What types of violations has Schweizer-Effax Gmbh received?

Schweizer-Effax Gmbh has been cited for 3 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 Schweizer-Effax Gmbh come from?

All FDA import refusal data for Schweizer-Effax 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.