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Arnet Pharmaceutical Corporation

⚠️ Moderate Risk

FEI: 1049842 • Davie, FL • UNITED STATES

FEI

FEI Number

1049842

📍

Location

Davie, FL

🇺🇸
🏢

Address

2525 Davie Rd Ste 330, , Davie, FL, United States

Moderate Risk

FDA Import Risk Assessment

49.5
LowModerateHighCritical

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

Statistics

8
Total Refusals
8
Unique Violations
7/2/2025
Latest Refusal
10/22/2001
Earliest Refusal

Score Breakdown

Violation Severity
51.7×40%
Refusal Volume
35.3×30%
Recency
89.3×20%
Frequency
3.4×10%
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

23004×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

4884×

HEALTH C

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling bears an unauthorized nutrient content/health claim.

4823×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

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).

38641×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

2561×

INCONSPICU

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

2181×

LIST INGRE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

Refusal History

DateProductViolationsDivision
7/2/2025
64DCL99EMOLLIENT, LUBRICANT, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
5/17/2024
54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
2300DIETARYLBL
3864NCONTACT
75UNAPPROVED
Division of Northern Border Imports (DNBI)
11/8/2016
54YCY99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
75UNAPPROVED
Division of Southeast Imports (DSEI)
7/21/2009
54YCE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
256INCONSPICU
New York District Office (NYK-DO)
10/17/2008
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2300DIETARYLBL
482NUTRIT LBL
488HEALTH C
New York District Office (NYK-DO)
10/17/2008
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2300DIETARYLBL
482NUTRIT LBL
488HEALTH C
New York District Office (NYK-DO)
10/17/2008
54FCH99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
2300DIETARYLBL
482NUTRIT LBL
488HEALTH C
New York District Office (NYK-DO)
10/22/2001
54YBE99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
320LACKS FIRM
488HEALTH C
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Arnet Pharmaceutical Corporation's FDA import refusal history?

Arnet Pharmaceutical Corporation (FEI: 1049842) has 8 FDA import refusal record(s) in our database, spanning from 10/22/2001 to 7/2/2025.

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. Arnet Pharmaceutical Corporation's FEI number is 1049842.

What types of violations has Arnet Pharmaceutical Corporation received?

Arnet Pharmaceutical Corporation has been cited for 8 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 Arnet Pharmaceutical Corporation come from?

All FDA import refusal data for Arnet Pharmaceutical Corporation 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.