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Glanbia Nutritionals

⚠️ Moderate Risk

FEI: 3005309236 • Corona, CA • UNITED STATES

FEI

FEI Number

3005309236

📍

Location

Corona, CA

🇺🇸
🏢

Address

484 Alcoa Cir, , Corona, CA, United States

Moderate Risk

FDA Import Risk Assessment

34.8
LowModerateHighCritical

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

Statistics

13
Total Refusals
10
Unique Violations
2/25/2013
Latest Refusal
12/15/2006
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
42.5×30%
Recency
0.0×20%
Frequency
21.0×10%
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

4828×

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.

3217×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

3067×

INSANITARY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.

2563×

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).

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.

831×

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)).

3291×

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
2/25/2013
54FCL99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
218LIST INGRE
473LABELING
482NUTRIT LBL
New York District Office (NYK-DO)
9/9/2011
54YBL99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
324NO ENGLISH
482NUTRIT LBL
New Orleans District Office (NOL-DO)
8/4/2008
20DCF99BERRY JUICE, N.E.C. BERRY JUICE OR CONCENTRATES
62NEEDS FCE
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/29/2007
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
256INCONSPICU
New York District Office (NYK-DO)
5/29/2007
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
256INCONSPICU
New York District Office (NYK-DO)
5/2/2007
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
256INCONSPICU
New York District Office (NYK-DO)
3/1/2007
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
306INSANITARY
321LACKS N/C
329JUICE %
482NUTRIT LBL
New York District Office (NYK-DO)
2/20/2007
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
1/22/2007
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
12/15/2006
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
12/15/2006
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
12/15/2006
21DHT01FRUIT COCTAIL, MIXED FRUIT, JUICES OR CONCENTRATES
306INSANITARY
321LACKS N/C
482NUTRIT LBL
New York District Office (NYK-DO)
12/15/2006
21DHT99MIXED FRUIT, JUICES OR CONCENTRATES N.E.C.,
306INSANITARY
321LACKS N/C
New York District Office (NYK-DO)

Frequently Asked Questions

What is Glanbia Nutritionals's FDA import refusal history?

Glanbia Nutritionals (FEI: 3005309236) has 13 FDA import refusal record(s) in our database, spanning from 12/15/2006 to 2/25/2013.

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. Glanbia Nutritionals's FEI number is 3005309236.

What types of violations has Glanbia Nutritionals received?

Glanbia Nutritionals has been cited for 10 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 Glanbia Nutritionals come from?

All FDA import refusal data for Glanbia Nutritionals 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.