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Sunnyland

⚠️ Moderate Risk

FEI: 3011281386 • Turnhout, Antwerp • BELGIUM

FEI

FEI Number

3011281386

📍

Location

Turnhout, Antwerp

🇧🇪

Country

BELGIUM
🏢

Address

Everdongenlaan 12, , Turnhout, Antwerp, Belgium

Moderate Risk

FDA Import Risk Assessment

37.2
LowModerateHighCritical

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

Statistics

14
Total Refusals
8
Unique Violations
4/26/2016
Latest Refusal
7/23/2014
Earliest Refusal

Score Breakdown

Violation Severity
40.4×40%
Refusal Volume
43.6×30%
Recency
0.0×20%
Frequency
79.5×10%
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

32913×

JUICE %

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 the food purports to be a beverage containing vegetable or fruit juice and does not bear a statement on the label in appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained therein.

48213×

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.

3246×

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)).

2605×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

834×

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.

2564×

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)).

621×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

3281×

USUAL NAME

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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.

Refusal History

DateProductViolationsDivision
4/26/2016
21VHT04GUAVA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
260FALSE
324NO ENGLISH
329JUICE %
482NUTRIT LBL
83NO PROCESS
New England District Office (NWE-DO)
4/26/2016
21VHT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
260FALSE
324NO ENGLISH
329JUICE %
482NUTRIT LBL
83NO PROCESS
New England District Office (NWE-DO)
4/26/2016
21VHT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
260FALSE
324NO ENGLISH
329JUICE %
482NUTRIT LBL
83NO PROCESS
New England District Office (NWE-DO)
1/19/2016
21VCT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
329JUICE %
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
1/19/2016
21VCT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
329JUICE %
482NUTRIT LBL
Southwest Import District Office (SWI-DO)
6/24/2015
21VCT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
328USUAL NAME
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
324NO ENGLISH
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
324NO ENGLISH
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT04GUAVA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
260FALSE
324NO ENGLISH
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT05MANGO, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
256INCONSPICU
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
256INCONSPICU
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT19LYCHEE, LICHEE, LITCHI, LEECHEE, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
256INCONSPICU
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/24/2015
21VCT04GUAVA, JUICE, MILK, CREME, DRINK OR NECTAR, SUB/TROPICAL FRUIT
256INCONSPICU
260FALSE
329JUICE %
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/23/2014
29AFF07SOFT DRINK, SUBTROPICAL OR TROPICAL FRUIT FLAVORED, NONCARBONATED
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Sunnyland's FDA import refusal history?

Sunnyland (FEI: 3011281386) has 14 FDA import refusal record(s) in our database, spanning from 7/23/2014 to 4/26/2016.

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. Sunnyland's FEI number is 3011281386.

What types of violations has Sunnyland received?

Sunnyland 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 Sunnyland come from?

All FDA import refusal data for Sunnyland 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.