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Shering Gmbh

⚠️ Moderate Risk

FEI: 3007993645 • Alemanha • GERMANY

FEI

FEI Number

3007993645

📍

Location

Alemanha

🇩🇪

Country

GERMANY
🏢

Address

Weimar-Turingia, , Alemanha, , Germany

Moderate Risk

FDA Import Risk Assessment

38.0
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
10/27/2011
Latest Refusal
8/8/2011
Earliest Refusal

Score Breakdown

Violation Severity
76.7×40%
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

752×

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).

1181×

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).

Refusal History

DateProductViolationsDivision
10/27/2011
64GDB27DESOGESTREL/ETHINYL ESTRADIOL (ESTROGEN)
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)
8/8/2011
64GCA07ESTRADIOL (ESTROGEN)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Shering Gmbh's FDA import refusal history?

Shering Gmbh (FEI: 3007993645) has 2 FDA import refusal record(s) in our database, spanning from 8/8/2011 to 10/27/2011.

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. Shering Gmbh's FEI number is 3007993645.

What types of violations has Shering Gmbh received?

Shering Gmbh 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 Shering Gmbh come from?

All FDA import refusal data for Shering 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.