Agroindustrias AIB
⚠️ Moderate Risk
FEI: 3004081837 • Lima • PERU
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
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
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.
WRONG IDEN
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 as defined in section 403(b) of the FD&C Act. The article appears to be offered for sale under the name of another food.
PESTICIDE2
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
OMITTED
The article is subject to refusal of admission pursuant Section 801(a)(3) of the FD&C Act in that it appears that a valuable constituent of the article has been in whole or in part omitted or abstracted from the article.
STD IDENT
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(g)(1) of the FD&C Act in that the article purports to be or is represented as a food for which a definition and standard of identity have been prescribed by regulations as provided by section 401 of the FD&C Act and the article does not conform to such definition and standard.
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.
SUBSTITUTE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears that a substance has been substituted wholly or in part for one or more of the article's ingredients.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/30/2014 | 20KGT04LEMON, CITRUS FRUIT JUICES OR CONCENTRATES | New York District Office (NYK-DO) | |
| 5/8/2012 | 24FEE04PIMIENTO PEPPER (FRUIT USED AS VEGETABLE) | 3721PESTICIDE2 | Los Angeles District Office (LOS-DO) |
| 7/25/2011 | 24FEE04PIMIENTO PEPPER (FRUIT USED AS VEGETABLE) | 2920PESTICIDES | Seattle District Office (SEA-DO) |
| 7/25/2011 | 24FEE04PIMIENTO PEPPER (FRUIT USED AS VEGETABLE) | 2920PESTICIDES | Seattle District Office (SEA-DO) |
| 7/25/2011 | 24FEE04PIMIENTO PEPPER (FRUIT USED AS VEGETABLE) | 2920PESTICIDES | Seattle District Office (SEA-DO) |
| 1/11/2008 | 24TEE01ARTICHOKE (LEAF & STEM VEGETABLE) | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Agroindustrias AIB's FDA import refusal history?
Agroindustrias AIB (FEI: 3004081837) has 6 FDA import refusal record(s) in our database, spanning from 1/11/2008 to 9/30/2014.
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. Agroindustrias AIB's FEI number is 3004081837.
What types of violations has Agroindustrias AIB received?
Agroindustrias AIB 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 Agroindustrias AIB come from?
All FDA import refusal data for Agroindustrias AIB 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.