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UNKNOWN MANUFACURER

⚠️ Moderate Risk

FEI: 3001810554 • UNKNOWN • PHILIPPINES

FEI

FEI Number

3001810554

📍

Location

UNKNOWN

🇵🇭
🏢

Address

UNKNOWN, , UNKNOWN, , Philippines

Moderate Risk

FDA Import Risk Assessment

43.0
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

3
Total Refusals
2
Unique Violations
2/9/2007
Latest Refusal
2/9/2007
Earliest Refusal

Score Breakdown

Violation Severity
83.3×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

752×

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).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

Refusal History

DateProductViolationsDivision
2/9/2007
60LCA99ANALGESIC, N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/9/2007
62GCA99ANTI-INFLAMMATORY N.E.C.
75UNAPPROVED
New Orleans District Office (NOL-DO)
2/9/2007
61TCA11MECLIZINE HCL (ANTI-EMETIC/NAUSEANT)
16DIRECTIONS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is UNKNOWN MANUFACURER's FDA import refusal history?

UNKNOWN MANUFACURER (FEI: 3001810554) has 3 FDA import refusal record(s) in our database, spanning from 2/9/2007 to 2/9/2007.

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. UNKNOWN MANUFACURER's FEI number is 3001810554.

What types of violations has UNKNOWN MANUFACURER received?

UNKNOWN MANUFACURER 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 UNKNOWN MANUFACURER come from?

All FDA import refusal data for UNKNOWN MANUFACURER 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.