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Lyocontract GmbH

⚠️ Moderate Risk

FEI: 3014034890 • Ilsenburg (Harz), Saxony-Anhalt • GERMANY

FEI

FEI Number

3014034890

📍

Location

Ilsenburg (Harz), Saxony-Anhalt

🇩🇪

Country

GERMANY
🏢

Address

Pulverwiese 1, , Ilsenburg (Harz), Saxony-Anhalt, Germany

Moderate Risk

FDA Import Risk Assessment

25.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
1/24/2022
Latest Refusal
1/24/2022
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
6.7×20%
Frequency
10.0×10%
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

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).

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

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
1/24/2022
66WAY99IMMUNOMODULATOR N.E.C.
118NOT LISTED
3280FRNMFGREG
333LACKS FIRM
335LACKS N/C
75UNAPPROVED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Lyocontract GmbH's FDA import refusal history?

Lyocontract GmbH (FEI: 3014034890) has 1 FDA import refusal record(s) in our database, spanning from 1/24/2022 to 1/24/2022.

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. Lyocontract GmbH's FEI number is 3014034890.

What types of violations has Lyocontract GmbH received?

Lyocontract GmbH has been cited for 5 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 Lyocontract GmbH come from?

All FDA import refusal data for Lyocontract 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.