Zolberg Corporation
⚠️ Moderate Risk
FEI: 3004200690 • Cavite, Calabarzon • PHILIPPINES
FEI Number
3004200690
Location
Cavite, Calabarzon
Country
PHILIPPINESAddress
168 Governor'S Drive, , Cavite, Calabarzon, Philippines
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
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.
DIRSEXMPT
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a drug within the meaning of Section 201(g) and it lacks adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 12/11/2024 | 62WAY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | Division of West Coast Imports (DWCI) | |
| 7/6/2022 | 62WBY16ALUM (ASTRINGENT/ANTI-PERSPIRANT) | Division of Northeast Imports (DNEI) | |
| 6/6/2022 | 62WBY99ASTRINGENT/ANTI-PERSPIRANT N.E.C. | Division of Northeast Imports (DNEI) |
Frequently Asked Questions
What is Zolberg Corporation's FDA import refusal history?
Zolberg Corporation (FEI: 3004200690) has 3 FDA import refusal record(s) in our database, spanning from 6/6/2022 to 12/11/2024.
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. Zolberg Corporation's FEI number is 3004200690.
What types of violations has Zolberg Corporation received?
Zolberg Corporation has been cited for 4 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 Zolberg Corporation come from?
All FDA import refusal data for Zolberg Corporation 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.