OGS/ OVERGOODS RETURNS
⚠️ High Risk
FEI: 3019158307 • Sao Paulo, Sao Paulo • BRAZIL
FEI Number
3019158307
Location
Sao Paulo, Sao Paulo
Country
BRAZILAddress
Rua Dom Aguirre, 554, , Sao Paulo, Sao Paulo, Brazil
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
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).
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).
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
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.
INCONSPICU
Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/15/2026 | 61MCY49CANNABIDIOL (ANTI-CONVULSANT) | Division of Southeast Imports (DSEI) | |
| 5/6/2024 | 54AIY99VITAMIN, N.E.C. | 238UNSAFE ADD | Division of Southeast Imports (DSEI) |
| 12/22/2023 | 66VDY99MISCELLANEOUS PATENT MEDICINES, ETC. | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 9/19/2023 | 66VIY99MISCELLANEOUS PATENT MEDICINES, ETC. | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is OGS/ OVERGOODS RETURNS's FDA import refusal history?
OGS/ OVERGOODS RETURNS (FEI: 3019158307) has 4 FDA import refusal record(s) in our database, spanning from 9/19/2023 to 1/15/2026.
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. OGS/ OVERGOODS RETURNS's FEI number is 3019158307.
What types of violations has OGS/ OVERGOODS RETURNS received?
OGS/ OVERGOODS RETURNS has been cited for 6 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 OGS/ OVERGOODS RETURNS come from?
All FDA import refusal data for OGS/ OVERGOODS RETURNS 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.