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Glenwood, LLC

⚠️ Moderate Risk

FEI: 2511504 • Englewood, NJ • UNITED STATES

FEI

FEI Number

2511504

📍

Location

Englewood, NJ

🇺🇸
🏢

Address

111 Cedar Ln, , Englewood, NJ, United States

Moderate Risk

FDA Import Risk Assessment

36.0
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
5/17/2013
Latest Refusal
12/30/2011
Earliest Refusal

Score Breakdown

Violation Severity
67.8×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
21.7×10%
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

753×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

1152×

DR QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to be represented as a drug the name of which is recognized in an official compendium and its strength appears to differ from or its quality or purity appear to fall below the standards set forth in such compendium.

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).

32802×

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.

Refusal History

DateProductViolationsDivision
5/17/2013
54BFE11POTASSIUM (MINERAL)
115DR QUALITY
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
New York District Office (NYK-DO)
5/17/2013
54BFE11POTASSIUM (MINERAL)
115DR QUALITY
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
New York District Office (NYK-DO)
12/30/2011
66VCE99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Glenwood, LLC's FDA import refusal history?

Glenwood, LLC (FEI: 2511504) has 3 FDA import refusal record(s) in our database, spanning from 12/30/2011 to 5/17/2013.

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. Glenwood, LLC's FEI number is 2511504.

What types of violations has Glenwood, LLC received?

Glenwood, LLC 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 Glenwood, LLC come from?

All FDA import refusal data for Glenwood, LLC 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.