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Inmedic Ab

✅ Low Risk

FEI: 3005354320 • Bredaryd • SWEDEN

FEI

FEI Number

3005354320

📍

Location

Bredaryd

🇸🇪

Country

SWEDEN
🏢

Address

Vastra Vagen, , Bredaryd, , Sweden

Low Risk

FDA Import Risk Assessment

24.9
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

3
Total Refusals
2
Unique Violations
11/27/2007
Latest Refusal
11/27/2007
Earliest Refusal

Score Breakdown

Violation Severity
38.0×40%
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

3413×

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).

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).

Refusal History

DateProductViolationsDivision
11/27/2007
76EJBHANDLE, INSTRUMENT, DENTAL
341REGISTERED
Los Angeles District Office (LOS-DO)
11/27/2007
76NRQBLADE-FROM ENDOSSEOUS DENTAL IMPLANT
118NOT LISTED
341REGISTERED
Los Angeles District Office (LOS-DO)
11/27/2007
76NRQBLADE-FROM ENDOSSEOUS DENTAL IMPLANT
118NOT LISTED
341REGISTERED
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Inmedic Ab's FDA import refusal history?

Inmedic Ab (FEI: 3005354320) has 3 FDA import refusal record(s) in our database, spanning from 11/27/2007 to 11/27/2007.

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. Inmedic Ab's FEI number is 3005354320.

What types of violations has Inmedic Ab received?

Inmedic Ab 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 Inmedic Ab come from?

All FDA import refusal data for Inmedic Ab 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.