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Advanced Technology Labs

⚠️ Moderate Risk

FEI: 1000657865 • Unterschleisheim, Bavaria • GERMANY

FEI

FEI Number

1000657865

📍

Location

Unterschleisheim, Bavaria

🇩🇪

Country

GERMANY
🏢

Address

Edisonstr. 6, , Unterschleisheim, Bavaria, Germany

Moderate Risk

FDA Import Risk Assessment

26.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
4
Unique Violations
12/20/2001
Latest Refusal
12/20/2001
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
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).

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).

471×

NON STD

The article is subject to refusal of admission pursuant to section 536(a) of the Federal Food, Drug, and Cosmetic Act (FFDCA) in that it appears to be an electronic product offered for importation into the United States which fails to comply with an applicable standard prescribed pursuant to section 534 of the FFDCA.

5081×

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.

Refusal History

DateProductViolationsDivision
12/20/2001
85LQTDOPPLER ULTRASOUND FOR FETAL EVALUATION
118NOT LISTED
341REGISTERED
47NON STD
508NO 510(K)
Baltimore District Office (BLT-DO)

Frequently Asked Questions

What is Advanced Technology Labs's FDA import refusal history?

Advanced Technology Labs (FEI: 1000657865) has 1 FDA import refusal record(s) in our database, spanning from 12/20/2001 to 12/20/2001.

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. Advanced Technology Labs's FEI number is 1000657865.

What types of violations has Advanced Technology Labs received?

Advanced Technology Labs 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 Advanced Technology Labs come from?

All FDA import refusal data for Advanced Technology Labs 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.