ANGAGA MARKET SA DE CV
⚠️ Moderate Risk
FEI: 3012753461 • Hermosillo • MEXICO
FEI Number
3012753461
Location
Hermosillo
Country
MEXICOAddress
Blvd. Abelardo L. Rodri, Centro, Hermosillo, , 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
STD QUALIT
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(h)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a standard of quality has been prescribed by regulation as provided by Section 401 of the FD&C Act, and its quality falls below such standard and its label does not bear a statement that it falls below such standard in such manner and form as such regulations specify.
FALSE
The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.
Refusal History
Frequently Asked Questions
What is ANGAGA MARKET SA DE CV's FDA import refusal history?
ANGAGA MARKET SA DE CV (FEI: 3012753461) has 2 FDA import refusal record(s) in our database, spanning from 11/23/2016 to 11/23/2016.
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. ANGAGA MARKET SA DE CV's FEI number is 3012753461.
What types of violations has ANGAGA MARKET SA DE CV received?
ANGAGA MARKET SA DE CV 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 ANGAGA MARKET SA DE CV come from?
All FDA import refusal data for ANGAGA MARKET SA DE CV 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.