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Vanka Kawat B.V.

⚠️ Moderate Risk

FEI: 3000304718 • Leidschendam • NETHERLANDS

FEI

FEI Number

3000304718

📍

Location

Leidschendam

🇳🇱
🏢

Address

Elbe 13-19, , Leidschendam, , Netherlands

Moderate Risk

FDA Import Risk Assessment

45.0
LowModerateHighCritical

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

Statistics

12
Total Refusals
2
Unique Violations
10/2/2007
Latest Refusal
8/5/2002
Earliest Refusal

Score Breakdown

Violation Severity
75.8×40%
Refusal Volume
41.3×30%
Recency
0.0×20%
Frequency
23.3×10%
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

8311×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

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)).

Refusal History

DateProductViolationsDivision
10/2/2007
28FGT99MIXED SPICE AND SEASONINGS, GROUND, CRACKED, WITHOUT SALT, N.E.C.
324NO ENGLISH
Los Angeles District Office (LOS-DO)
9/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
9/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)
8/5/2002
27YGE06PEPPER SAUCE (HOT, MILD, ETC.)
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Vanka Kawat B.V.'s FDA import refusal history?

Vanka Kawat B.V. (FEI: 3000304718) has 12 FDA import refusal record(s) in our database, spanning from 8/5/2002 to 10/2/2007.

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. Vanka Kawat B.V.'s FEI number is 3000304718.

What types of violations has Vanka Kawat B.V. received?

Vanka Kawat B.V. has been cited for 2 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 Vanka Kawat B.V. come from?

All FDA import refusal data for Vanka Kawat B.V. 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.