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Orbitalum Tools Gmbh

⚠️ Moderate Risk

FEI: 3008325899 • Singen (Hohentwiel), Baden-Wurttemberg • GERMANY

FEI

FEI Number

3008325899

📍

Location

Singen (Hohentwiel), Baden-Wurttemberg

🇩🇪

Country

GERMANY
🏢

Address

Josef-Schuttler-Str. 17, , Singen (Hohentwiel), Baden-Wurttemberg, Germany

Moderate Risk

FDA Import Risk Assessment

26.7
LowModerateHighCritical

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

Statistics

1
Total Refusals
5
Unique Violations
7/1/2010
Latest Refusal
7/1/2010
Earliest Refusal

Score Breakdown

Violation Severity
56.0×40%
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

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2781×

NO TAG

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 to which is not affixed a certification in the form of a label or tag in conformity with section 534(h).

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

3441×

WARNINGS

It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.

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.

Refusal History

DateProductViolationsDivision
7/1/2010
95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
16DIRECTIONS
278NO TAG
333LACKS FIRM
344WARNINGS
47NON STD
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Orbitalum Tools Gmbh's FDA import refusal history?

Orbitalum Tools Gmbh (FEI: 3008325899) has 1 FDA import refusal record(s) in our database, spanning from 7/1/2010 to 7/1/2010.

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. Orbitalum Tools Gmbh's FEI number is 3008325899.

What types of violations has Orbitalum Tools Gmbh received?

Orbitalum Tools Gmbh 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 Orbitalum Tools Gmbh come from?

All FDA import refusal data for Orbitalum Tools 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.