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B E Meyers & Co Inc Electro Optics

⚠️ Moderate Risk

FEI: 3004496941 • Redmond, WA • UNITED STATES

FEI

FEI Number

3004496941

📍

Location

Redmond, WA

🇺🇸
🏢

Address

14540 NE 91st St, , Redmond, WA, United States

Moderate Risk

FDA Import Risk Assessment

32.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
1
Unique Violations
6/22/2009
Latest Refusal
6/22/2009
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
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

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
6/22/2009
95RESLASER POINTER, SURVEYING, LEVELING, ALIGNMENT LASER PRODUCTS
47NON STD
New York District Office (NYK-DO)

Frequently Asked Questions

What is B E Meyers & Co Inc Electro Optics's FDA import refusal history?

B E Meyers & Co Inc Electro Optics (FEI: 3004496941) has 1 FDA import refusal record(s) in our database, spanning from 6/22/2009 to 6/22/2009.

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. B E Meyers & Co Inc Electro Optics's FEI number is 3004496941.

What types of violations has B E Meyers & Co Inc Electro Optics received?

B E Meyers & Co Inc Electro Optics 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 B E Meyers & Co Inc Electro Optics come from?

All FDA import refusal data for B E Meyers & Co Inc Electro Optics 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.