COMERCIALIZADORA GLOBAL TRADINGSPA
⚠️ Moderate Risk
FEI: 3014701437 • Vitacura, Region Metropolitana De Santia • CHILE
FEI Number
3014701437
Location
Vitacura, Region Metropolitana De Santia
Country
CHILEAddress
Avenida Vitacura 3568, Of 807, , Vitacura, Region Metropolitana De Santia, Chile
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
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)).
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/21/2022 | 24FHI08PEPPER, HOT, N.E.C. (FRUIT USED AS VEGETABLE) | Division of Southeast Imports (DSEI) | |
| 8/25/2021 | 16MCT09OCTOPUS, OTHER AQUATIC SPECIES | Division of Southeast Imports (DSEI) | |
| 6/29/2021 | 31AVT03COFFEE, INSTANT | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/29/2021 | 24NGD39HEART OF PALM (MICROGREEN) | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/29/2021 | 25JGD06POTATO (ROOT & TUBER VEGETABLE) | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/29/2021 | 24BGD60CORN, DRIED OR PASTE | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/29/2021 | 24EGD14STRINGBEANS, BEAN AND PEA SPROUTS | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/29/2021 | 24AGD22MIXED BEAN/SEED SPROUTS | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
| 6/29/2021 | 24EGD14STRINGBEANS, BEAN AND PEA SPROUTS | 324NO ENGLISH | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is COMERCIALIZADORA GLOBAL TRADINGSPA's FDA import refusal history?
COMERCIALIZADORA GLOBAL TRADINGSPA (FEI: 3014701437) has 9 FDA import refusal record(s) in our database, spanning from 6/29/2021 to 9/21/2022.
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. COMERCIALIZADORA GLOBAL TRADINGSPA's FEI number is 3014701437.
What types of violations has COMERCIALIZADORA GLOBAL TRADINGSPA received?
COMERCIALIZADORA GLOBAL TRADINGSPA 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 COMERCIALIZADORA GLOBAL TRADINGSPA come from?
All FDA import refusal data for COMERCIALIZADORA GLOBAL TRADINGSPA 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.