ImportRefusal LogoImportRefusal

Alka Loid Ad

⚠️ Moderate Risk

FEI: 3006331772 • Skoplje • MACEDONIA

FEI

FEI Number

3006331772

📍

Location

Skoplje

🇲🇰

Country

MACEDONIA
🏢

Address

Bul A Makedonski 12, , Skoplje, , Macedonia

Moderate Risk

FDA Import Risk Assessment

42.9
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
5/14/2020
Latest Refusal
7/5/2007
Earliest Refusal

Score Breakdown

Violation Severity
90.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
2.3×10%
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

753×

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).

Refusal History

DateProductViolationsDivision
5/14/2020
62UDY19PHOLCODINE (ANTI-TUSSIVE/COLD)
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/5/2007
56BDN05AMPICILLIN (PENICILLIN, SYNTHETICALLY PRODUCED)
75UNAPPROVED
New Orleans District Office (NOL-DO)
7/5/2007
56BDZ03AMOXICILLIN TRIHYDRATE (PENICILLIN, SYNTHETICALLY PRODUCED)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Alka Loid Ad's FDA import refusal history?

Alka Loid Ad (FEI: 3006331772) has 3 FDA import refusal record(s) in our database, spanning from 7/5/2007 to 5/14/2020.

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. Alka Loid Ad's FEI number is 3006331772.

What types of violations has Alka Loid Ad received?

Alka Loid Ad has been cited for 1 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 Alka Loid Ad come from?

All FDA import refusal data for Alka Loid Ad 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.