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Electro-Med Health Industries

⚠️ Moderate Risk

FEI: 1028751 • North Miami, FL • UNITED STATES

FEI

FEI Number

1028751

📍

Location

North Miami, FL

🇺🇸
🏢

Address

11601 Biscayne Blvd Ste 200A, , North Miami, FL, United States

Moderate Risk

FDA Import Risk Assessment

30.6
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
3/13/2006
Latest Refusal
3/13/2006
Earliest Refusal

Score Breakdown

Violation Severity
58.3×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

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).

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.

1261×

FAILS STD

The article appears to be a device which is subject to a performance standard established under Section 514 and does not appear to be in all respects in conformity with such standard.

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).

Refusal History

DateProductViolationsDivision
3/13/2006
90IYNSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
118NOT LISTED
508NO 510(K)
Cincinnati District Office (CIN-DO)
3/13/2006
84GZODEVICE, GALVANIC SKIN RESPONSE MEASUREMENT
118NOT LISTED
126FAILS STD
341REGISTERED
508NO 510(K)
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Electro-Med Health Industries's FDA import refusal history?

Electro-Med Health Industries (FEI: 1028751) has 2 FDA import refusal record(s) in our database, spanning from 3/13/2006 to 3/13/2006.

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. Electro-Med Health Industries's FEI number is 1028751.

What types of violations has Electro-Med Health Industries received?

Electro-Med Health Industries 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 Electro-Med Health Industries come from?

All FDA import refusal data for Electro-Med Health Industries 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.