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Fisba Optik Ag

✅ Low Risk

FEI: 3002184548 • Saint Gall, Saint Gall • SWITZERLAND

FEI

FEI Number

3002184548

📍

Location

Saint Gall, Saint Gall

🇨🇭
🏢

Address

Rorschacher Strasse 268, , Saint Gall, Saint Gall, Switzerland

Low Risk

FDA Import Risk Assessment

24.5
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
10/21/2013
Latest Refusal
9/1/2004
Earliest Refusal

Score Breakdown

Violation Severity
47.5×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
2.2×10%
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).

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.

37411×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

4761×

NO REGISTR

The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).

Refusal History

DateProductViolationsDivision
10/21/2013
78KOGENDOSCOPE AND/OR ACCESSORIES
118NOT LISTED
3280FRNMFGREG
3741FRNMFGREG
Detroit District Office (DET-DO)
9/1/2004
95L22LASER PRODUCT FOR NON-MEDICAL USE
476NO REGISTR
New York District Office (NYK-DO)

Frequently Asked Questions

What is Fisba Optik Ag's FDA import refusal history?

Fisba Optik Ag (FEI: 3002184548) has 2 FDA import refusal record(s) in our database, spanning from 9/1/2004 to 10/21/2013.

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. Fisba Optik Ag's FEI number is 3002184548.

What types of violations has Fisba Optik Ag received?

Fisba Optik Ag 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 Fisba Optik Ag come from?

All FDA import refusal data for Fisba Optik Ag 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.