Hibrid D.O.O.
⚠️ Moderate Risk
FEI: 3010933339 • Gornja Dobrinja, Zlatibor • SERBIA
FEI Number
3010933339
Location
Gornja Dobrinja, Zlatibor
Country
SERBIAAddress
Gornja Dobrinja, , Gornja Dobrinja, Zlatibor, Serbia
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
MFR INJ
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act (the Act) in that such article appears to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
HEPATITISA
The article is subject to refusal of admission to pursuant Section 801(a)(3) in that it appears to contain Hepatitis A Virus, a poisonous or deleterious substance which may render it injurious to health.
MFR INSAN
The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.
Refusal History
Frequently Asked Questions
What is Hibrid D.O.O.'s FDA import refusal history?
Hibrid D.O.O. (FEI: 3010933339) has 2 FDA import refusal record(s) in our database, spanning from 12/11/2019 to 8/25/2020.
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. Hibrid D.O.O.'s FEI number is 3010933339.
What types of violations has Hibrid D.O.O. received?
Hibrid D.O.O. 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 Hibrid D.O.O. come from?
All FDA import refusal data for Hibrid D.O.O. 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.