GALDISA SA DE CV (P3)
⚠️ Moderate Risk
FEI: 3012747158 • Ciudad De Mexico • MEXICO
FEI Number
3012747158
Location
Ciudad De Mexico
Country
MEXICOAddress
Filomeno Mata 922, Col. Santa Maria Aztahuacan, Iztapalapa, Ciudad De Mexico, , 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
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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:
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
AFLATOXIN
The article appears to contain a mycotoxin, a poisonous and deleterious substance which may render it injurious to health.
SALMONELLA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/17/2019 | 72CHH99PET BIRD FOOD N.E.C. | 241PESTICIDE | Division of Southwest Imports (DSWI) |
| 8/31/2018 | 72CHH99PET BIRD FOOD N.E.C. | Division of Southwest Imports (DSWI) | |
| 12/10/2009 | 23YYY99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C. | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 11/6/2009 | 23YYY99NUTS OR EDIBLE SEEDS NOT MENTIONED ELSEWHERE, N.E.C. | 238UNSAFE ADD | Southwest Import District Office (SWI-DO) |
| 8/27/2009 | 23BGT07PEANUT, SHELLED | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 8/11/2009 | 23BGT07PEANUT, SHELLED | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 3/6/2007 | 23BGP07PEANUT, SHELLED | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 1/29/2007 | 23BGP07PEANUT, SHELLED | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 1/29/2007 | 24EGP05FAVA BEAN, BEAN AND PEA SPROUTS | 11UNSAFE COL | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is GALDISA SA DE CV (P3)'s FDA import refusal history?
GALDISA SA DE CV (P3) (FEI: 3012747158) has 9 FDA import refusal record(s) in our database, spanning from 1/29/2007 to 1/17/2019.
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. GALDISA SA DE CV (P3)'s FEI number is 3012747158.
What types of violations has GALDISA SA DE CV (P3) received?
GALDISA SA DE CV (P3) has been cited for 7 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 GALDISA SA DE CV (P3) come from?
All FDA import refusal data for GALDISA SA DE CV (P3) 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.