Vital Maycar S.A.
⚠️ Moderate Risk
FEI: 3006807927 • Buenos Aires • ARGENTINA
FEI Number
3006807927
Location
Buenos Aires
Country
ARGENTINAAddress
San Justo Av., Mso. Bufano, , Buenos Aires, , Argentina
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
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).
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.
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.
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.
TRANSFAT
The product is misbranded under Section 403(q) because the nutrition label does not provide all of the information required by 21 CFR 101.9(c); specifically, the label does not bear the amount of trans fat [21 CFR 101.9(c)(2)(ii)].
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/31/2008 | 24DGE22MIXED BEAN/SEED SPROUTS, JUICE OR DRINK | Los Angeles District Office (LOS-DO) | |
| 10/31/2008 | 24DGE22MIXED BEAN/SEED SPROUTS, JUICE OR DRINK | Los Angeles District Office (LOS-DO) | |
| 10/31/2008 | 24DGE22MIXED BEAN/SEED SPROUTS, JUICE OR DRINK | Los Angeles District Office (LOS-DO) | |
| 10/31/2008 | 24DGE22MIXED BEAN/SEED SPROUTS, JUICE OR DRINK | Los Angeles District Office (LOS-DO) | |
| 10/31/2008 | 24DGE22MIXED BEAN/SEED SPROUTS, JUICE OR DRINK | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Vital Maycar S.A.'s FDA import refusal history?
Vital Maycar S.A. (FEI: 3006807927) has 5 FDA import refusal record(s) in our database, spanning from 10/31/2008 to 10/31/2008.
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. Vital Maycar S.A.'s FEI number is 3006807927.
What types of violations has Vital Maycar S.A. received?
Vital Maycar S.A. has been cited for 6 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 Vital Maycar S.A. come from?
All FDA import refusal data for Vital Maycar S.A. 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.