Unilab
⚠️ High Risk
FEI: 3003899848 • Mandaluyong • PHILIPPINES
FEI Number
3003899848
Location
Mandaluyong
Country
PHILIPPINESAddress
66 United St, , Mandaluyong, , Philippines
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 2/28/2025 | 60CDA09PHENYLEPHRINE HCL (ADRENERGIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 2/28/2025 | 60LCA01ACETAMINOPHEN (ANALGESIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 8/9/2024 | 60XDY02METOPROLOL (ANTI-ADRENERGIC) | 75UNAPPROVED | Division of Southeast Imports (DSEI) |
| 1/4/2011 | 60SBA04ALUMINUM HYDROXIDE (ANTACID) | 75UNAPPROVED | New Orleans District Office (NOL-DO) |
| 7/20/2005 | 60XDB17ATENOLOL (ANTI-ADRENERGIC) | 118NOT LISTED | San Francisco District Office (SAN-DO) |
| 7/20/2005 | 61GDY50SULFADOXINE (ANTI-BACTERIAL) (NOT ANTIBIOTIC) | 118NOT LISTED | San Francisco District Office (SAN-DO) |
Frequently Asked Questions
What is Unilab's FDA import refusal history?
Unilab (FEI: 3003899848) has 6 FDA import refusal record(s) in our database, spanning from 7/20/2005 to 2/28/2025.
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. Unilab's FEI number is 3003899848.
What types of violations has Unilab received?
Unilab has been cited for 2 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 Unilab come from?
All FDA import refusal data for Unilab 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.