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FM MEIN ARZTBEDARF GMBH

⚠️ High Risk

FEI: 3030310113 • Hall In Tirol, Tyrol • AUSTRIA

FEI

FEI Number

3030310113

📍

Location

Hall In Tirol, Tyrol

🇦🇹

Country

AUSTRIA
🏢

Address

Schloglstrase 57, , Hall In Tirol, Tyrol, Austria

High Risk

FDA Import Risk Assessment

51.0
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

2
Total Refusals
4
Unique Violations
10/29/2025
Latest Refusal
7/3/2025
Earliest Refusal

Score Breakdown

Violation Severity
61.7×40%
Refusal Volume
17.7×30%
Recency
95.4×20%
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

1182×

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).

5082×

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.

2371×

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).

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.

Refusal History

DateProductViolationsDivision
10/29/2025
88PPMGENERAL PURPOSE REAGENT
118NOT LISTED
237NO PMA
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/3/2025
83QWBOVER-THE-COUNTER MOLECULAR TEST TO DETECT SARS-COV-2
118NOT LISTED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is FM MEIN ARZTBEDARF GMBH's FDA import refusal history?

FM MEIN ARZTBEDARF GMBH (FEI: 3030310113) has 2 FDA import refusal record(s) in our database, spanning from 7/3/2025 to 10/29/2025.

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. FM MEIN ARZTBEDARF GMBH's FEI number is 3030310113.

What types of violations has FM MEIN ARZTBEDARF GMBH received?

FM MEIN ARZTBEDARF GMBH has been cited for 4 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 FM MEIN ARZTBEDARF GMBH come from?

All FDA import refusal data for FM MEIN ARZTBEDARF GMBH 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.