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Abic Ltd.

⚠️ Moderate Risk

FEI: 3002806283 • Netanya • ISRAEL

FEI

FEI Number

3002806283

📍

Location

Netanya

🇮🇱

Country

ISRAEL
🏢

Address

New Industrial Zone, Pob 8077, Kiryat Sapir, Netanya, , Israel

Moderate Risk

FDA Import Risk Assessment

37.5
LowModerateHighCritical

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

Statistics

6
Total Refusals
4
Unique Violations
7/6/2012
Latest Refusal
9/18/2003
Earliest Refusal

Score Breakdown

Violation Severity
68.6×40%
Refusal Volume
31.3×30%
Recency
0.0×20%
Frequency
6.8×10%
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

754×

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).

1181×

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).

3241×

NO ENGLISH

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)).

4821×

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.

Refusal History

DateProductViolationsDivision
7/6/2012
64BCA25HYDROCHLOROTHIAZIDE (DIURETIC)
75UNAPPROVED
New Orleans District Office (NOL-DO)
3/12/2009
64TDS02GLATIRAMER ACETATE (IMMUNOSUPPRESSIVE)
75UNAPPROVED
New York District Office (NYK-DO)
3/12/2009
64TDP02GLATIRAMER ACETATE (IMMUNOSUPPRESSIVE)
75UNAPPROVED
New York District Office (NYK-DO)
3/27/2007
61JDB16ROSUVASTATIN CALCIUM
75UNAPPROVED
New Orleans District Office (NOL-DO)
12/27/2005
62OCB24DILTIAZEM HYDROCHLORIDE (ANTI-HYPERTENSIVE - PART II)
118NOT LISTED
San Francisco District Office (SAN-DO)
9/18/2003
54ABY90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Abic Ltd.'s FDA import refusal history?

Abic Ltd. (FEI: 3002806283) has 6 FDA import refusal record(s) in our database, spanning from 9/18/2003 to 7/6/2012.

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. Abic Ltd.'s FEI number is 3002806283.

What types of violations has Abic Ltd. received?

Abic Ltd. 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 Abic Ltd. come from?

All FDA import refusal data for Abic Ltd. 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.