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Ad-Tech Medical Instrument Corporation

✅ Low Risk

FEI: 2183456 • Oak Creek, WI • UNITED STATES

FEI

FEI Number

2183456

📍

Location

Oak Creek, WI

🇺🇸
🏢

Address

400 W Oakview Pkwy, , Oak Creek, WI, United States

Low Risk

FDA Import Risk Assessment

24.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
8/17/2020
Latest Refusal
8/17/2020
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1181×

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
8/17/2020
79FTYTAPE, MEASURING, RULERS AND CALIPERS
118NOT LISTED
Division of Northern Border Imports (DNBI)

Frequently Asked Questions

What is Ad-Tech Medical Instrument Corporation's FDA import refusal history?

Ad-Tech Medical Instrument Corporation (FEI: 2183456) has 1 FDA import refusal record(s) in our database, spanning from 8/17/2020 to 8/17/2020.

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. Ad-Tech Medical Instrument Corporation's FEI number is 2183456.

What types of violations has Ad-Tech Medical Instrument Corporation received?

Ad-Tech Medical Instrument Corporation 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 Ad-Tech Medical Instrument Corporation come from?

All FDA import refusal data for Ad-Tech Medical Instrument Corporation 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.