Zuccari srl
⚠️ Moderate Risk
FEI: 3004737414 • Trento, Trento • ITALY
FEI Number
3004737414
Location
Trento, Trento
Country
ITALYAddress
Via del Commercio 66/68, , Trento, Trento, Italy
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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)).
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.
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.
NO ENGLISH
Required label or labeling appears to not be in English in violation of 21 C.F.R. 201.15(c)(1).
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
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).
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/2/2015 | 66VBL99MISCELLANEOUS PATENT MEDICINES, ETC. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 66VBJ99MISCELLANEOUS PATENT MEDICINES, ETC. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 53JD02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 53JD02DEODORANTS (UNDERARM)(NOT ANTIPERSPIRANT) (PERSONAL CLEANLINESS) | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54KAL08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED)) | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54FEL99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54KAL08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED)) | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 31GYY99COFFEE READY TO DRINK, N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54KYY08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED)) | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54KYY08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED)) | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54FER99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54FEL99HERBALS & BOTANICALS (NOT TEAS), N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 30YGH99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 30YHT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 30YHT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 30YHT99BEVERAGE BASE NOT MENTIONED ELSEWHERE, N.E.C. | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 21VHT48COCONUT, SUBTROPICAL AND TROPICAL FRUIT, JUICES, MILK, CREME, DRINKS AND NECTARS | Chicago District Office (CHI-DO) | |
| 11/2/2015 | 54KYY08ALOE (HERBAL AND BOTANICAL (NOT TEAS) II (CONTINUED)) | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Zuccari srl's FDA import refusal history?
Zuccari srl (FEI: 3004737414) has 18 FDA import refusal record(s) in our database, spanning from 11/2/2015 to 11/2/2015.
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. Zuccari srl's FEI number is 3004737414.
What types of violations has Zuccari srl received?
Zuccari srl has been cited for 9 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 Zuccari srl come from?
All FDA import refusal data for Zuccari srl 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.