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Olympus Corp

⚠️ Moderate Risk

FEI: 1000549845 • New Hyde Park, NY • UNITED STATES

FEI

FEI Number

1000549845

📍

Location

New Hyde Park, NY

🇺🇸
🏢

Address

4 Nevada Dr, , New Hyde Park, NY, United States

Moderate Risk

FDA Import Risk Assessment

27.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
3/20/2020
Latest Refusal
8/14/2007
Earliest Refusal

Score Breakdown

Violation Severity
51.4×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
2.4×10%
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

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).

3412×

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).

5082×

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.

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
3/20/2020
78GCPENDOSCOPE, AC-POWERED AND ACCESSORIES
118NOT LISTED
341REGISTERED
508NO 510(K)
Division of Northern Border Imports (DNBI)
7/21/2017
79FSWLIGHT, SURGICAL, ENDOSCOPIC
341REGISTERED
Division of Northern Border Imports (DNBI)
8/14/2007
78FDTDUODEDOSCOPE, ESOPHAGO GASTRO
118NOT LISTED
476NO REGISTR
508NO 510(K)
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Olympus Corp's FDA import refusal history?

Olympus Corp (FEI: 1000549845) has 3 FDA import refusal record(s) in our database, spanning from 8/14/2007 to 3/20/2020.

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. Olympus Corp's FEI number is 1000549845.

What types of violations has Olympus Corp received?

Olympus Corp 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 Olympus Corp come from?

All FDA import refusal data for Olympus Corp 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.