Bielita Ltd
⚠️ Moderate Risk
FEI: 3006568638 • Minsk, Minsk • BELARUS
FEI Number
3006568638
Location
Minsk, Minsk
Country
BELARUSAddress
Dekabristov 29a, , Minsk, Minsk, Belarus
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/5/2010 | 53EC06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | New York District Office (NYK-DO) | |
| 5/5/2010 | 53EC06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING) | New York District Office (NYK-DO) | |
| 5/5/2010 | 53LC06MOISTURIZING (SKIN CARE PREPARATIONS) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Bielita Ltd's FDA import refusal history?
Bielita Ltd (FEI: 3006568638) has 3 FDA import refusal record(s) in our database, spanning from 5/5/2010 to 5/5/2010.
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. Bielita Ltd's FEI number is 3006568638.
What types of violations has Bielita Ltd received?
Bielita Ltd 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 Bielita Ltd come from?
All FDA import refusal data for Bielita Ltd 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.