COLIMAN DISTRIBUIDORES S.A. DE C.V.
⚠️ Moderate Risk
FEI: 3004294356 • TIJUANA, MX-BCN • MEXICO
FEI Number
3004294356
Location
TIJUANA, MX-BCN
Country
MEXICOAddress
Ave. Ermita 193-a, , TIJUANA, MX-BCN, 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
PESTICIDE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain a pesticide chemical residue, which causes the article to be adulterated within the meaning of section 402(a)(2)(B) of the FD&C Act. Bears or contains:
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/4/2007 | 24TFB99LEAF & STEM VEGETABLES, N.E.C. | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 4/20/2006 | 21SFB06PAPAYA (PAPAW) (SUBTROPICAL AND TROPICAL FRUIT) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
| 11/18/2003 | 21SFC06PAPAYA (PAPAW) (SUBTROPICAL AND TROPICAL FRUIT) | 241PESTICIDE | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is COLIMAN DISTRIBUIDORES S.A. DE C.V.'s FDA import refusal history?
COLIMAN DISTRIBUIDORES S.A. DE C.V. (FEI: 3004294356) has 3 FDA import refusal record(s) in our database, spanning from 11/18/2003 to 1/4/2007.
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. COLIMAN DISTRIBUIDORES S.A. DE C.V.'s FEI number is 3004294356.
What types of violations has COLIMAN DISTRIBUIDORES S.A. DE C.V. received?
COLIMAN DISTRIBUIDORES S.A. DE C.V. has been cited for 1 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 COLIMAN DISTRIBUIDORES S.A. DE C.V. come from?
All FDA import refusal data for COLIMAN DISTRIBUIDORES S.A. DE C.V. 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.