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Dr J Hansler

⚠️ Moderate Risk

FEI: 3002862267 • Iffezheim, Baden-Wurttemberg • GERMANY

FEI

FEI Number

3002862267

📍

Location

Iffezheim, Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Nordring 8, , Iffezheim, Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

31.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
5
Unique Violations
8/27/2021
Latest Refusal
8/7/2012
Earliest Refusal

Score Breakdown

Violation Severity
58.9×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
4.4×10%
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

1183×

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).

5083×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

32801×

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.

3411×

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).

751×

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
8/27/2021
80FMFSYRINGE, PISTON
118NOT LISTED
3280FRNMFGREG
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
8/7/2012
80FPASET, ADMINISTRATION, INTRAVASCULAR
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
8/7/2012
80FPASET, ADMINISTRATION, INTRAVASCULAR
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
8/7/2012
60IDN12SODIUM CITRATE (ALKALIZER)
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Dr J Hansler's FDA import refusal history?

Dr J Hansler (FEI: 3002862267) has 4 FDA import refusal record(s) in our database, spanning from 8/7/2012 to 8/27/2021.

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. Dr J Hansler's FEI number is 3002862267.

What types of violations has Dr J Hansler received?

Dr J Hansler has been cited for 5 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 Dr J Hansler come from?

All FDA import refusal data for Dr J Hansler 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.