Vidamar Guadalajara
⚠️ Moderate Risk
FEI: 3003899415 • Guadalajara • MEXICO
FEI Number
3003899415
Location
Guadalajara
Country
MEXICOAddress
Mgrcadao De Pescp, , Guadalajara, , Mexico
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
DIETARYLBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.
NUTRIT LBL
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/25/2003 | 54HCH04FISH OIL (FATS AND LIPID SUBSTANCES) | Seattle District Office (SEA-DO) | |
| 2/25/2003 | 54HCH04FISH OIL (FATS AND LIPID SUBSTANCES) | Seattle District Office (SEA-DO) | |
| 2/25/2003 | 54HCH04FISH OIL (FATS AND LIPID SUBSTANCES) | Seattle District Office (SEA-DO) |
Frequently Asked Questions
What is Vidamar Guadalajara's FDA import refusal history?
Vidamar Guadalajara (FEI: 3003899415) has 3 FDA import refusal record(s) in our database, spanning from 2/25/2003 to 2/25/2003.
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. Vidamar Guadalajara's FEI number is 3003899415.
What types of violations has Vidamar Guadalajara received?
Vidamar Guadalajara 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 Vidamar Guadalajara come from?
All FDA import refusal data for Vidamar Guadalajara 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.