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Allanmar International Company

⚠️ Moderate Risk

FEI: 3008327592 • Santa Fe • ARGENTINA

FEI

FEI Number

3008327592

📍

Location

Santa Fe

🇦🇷

Country

ARGENTINA
🏢

Address

H De La Quintana 827, , Santa Fe, , Argentina

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
2
Unique Violations
6/18/2012
Latest Refusal
6/18/2012
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

3412×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

Refusal History

DateProductViolationsDivision
6/18/2012
89MOZACID, HYALURONIC, INTRAARTICULAR
237NO PMA
341REGISTERED
New Orleans District Office (NOL-DO)
6/18/2012
89MOZACID, HYALURONIC, INTRAARTICULAR
237NO PMA
341REGISTERED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Allanmar International Company's FDA import refusal history?

Allanmar International Company (FEI: 3008327592) has 2 FDA import refusal record(s) in our database, spanning from 6/18/2012 to 6/18/2012.

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. Allanmar International Company's FEI number is 3008327592.

What types of violations has Allanmar International Company received?

Allanmar International Company 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 Allanmar International Company come from?

All FDA import refusal data for Allanmar International Company 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.