Marco Marin Idrovo
⚠️ High Risk
FEI: 3004742361 • Guayaquil, Guayas • ECUADOR
FEI Number
3004742361
Location
Guayaquil, Guayas
Country
ECUADORAddress
Cola Paraiso Chirimdya 5, , Guayaquil, Guayas, Ecuador
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
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
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
UNAPPROVED
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).
NO ENGLISH
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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/6/2004 | 60LAJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) | |
| 11/8/2004 | 54ABA13VITAMIN C (ASCORBIC ACID) | 324NO ENGLISH | New York District Office (NYK-DO) |
| 11/8/2004 | 60SAL14MAGNESIUM HYDROXIDE (ANTACID) | New York District Office (NYK-DO) | |
| 11/8/2004 | 63HAA23SENNOSIDES A AND B (CATHARTIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LBJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LBJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) | |
| 11/8/2004 | 60CAK51TETRAHYDROZOLINE HCL (ADRENERGIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LBA05ASPIRIN (ANALGESIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LAA05ASPIRIN (ANALGESIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LAA01ACETAMINOPHEN (ANALGESIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LBI01ACETAMINOPHEN (ANALGESIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LBJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) | |
| 11/8/2004 | 60SBA99ANTACID, N.E.C. | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LBI01ACETAMINOPHEN (ANALGESIC) | New York District Office (NYK-DO) | |
| 11/8/2004 | 60LAJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Marco Marin Idrovo's FDA import refusal history?
Marco Marin Idrovo (FEI: 3004742361) has 15 FDA import refusal record(s) in our database, spanning from 11/8/2004 to 12/6/2004.
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. Marco Marin Idrovo's FEI number is 3004742361.
What types of violations has Marco Marin Idrovo received?
Marco Marin Idrovo 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 Marco Marin Idrovo come from?
All FDA import refusal data for Marco Marin Idrovo 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.