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Miracilum S.A.

✅ Low Risk

FEI: 3003232696 • Cracow, Malopolskie • POLAND

FEI

FEI Number

3003232696

📍

Location

Cracow, Malopolskie

🇵🇱

Country

POLAND
🏢

Address

Ul. Zablocie 23, , Cracow, Malopolskie, Poland

Low Risk

FDA Import Risk Assessment

20.3
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

1
Total Refusals
3
Unique Violations
4/11/2013
Latest Refusal
4/11/2013
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
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

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

4741×

COSMETLBLG

It appears the label does not bear the common or usual name of the cosmetic.

4751×

COSMETLBLG

It appears that the cosmetic consists of two or more ingredients and the label does not list the common or usual name of each ingredient.

Refusal History

DateProductViolationsDivision
4/11/2013
53LD03FACE,BODY,AND HAND (EXCLUDING SHAVING PREPARATIONS) (SKIN CARE PREPARATIONS)
473LABELING
474COSMETLBLG
475COSMETLBLG
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Miracilum S.A.'s FDA import refusal history?

Miracilum S.A. (FEI: 3003232696) has 1 FDA import refusal record(s) in our database, spanning from 4/11/2013 to 4/11/2013.

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. Miracilum S.A.'s FEI number is 3003232696.

What types of violations has Miracilum S.A. received?

Miracilum S.A. 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 Miracilum S.A. come from?

All FDA import refusal data for Miracilum S.A. 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.