Alimentic SAS
FDA import alert and refusal historyBogota, ColombiaFEI 3008904124
Recorded by FDA as ALIMENTIC SAS
As of October 25, 2026, Alimentic SAS (Bogota, Colombia) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for achiras huilenses celio cheese biscuit, published by FDA on November 6, 2017, is also listed on Import Alert 99-22 (red list), and has 10 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red listIA 99-22 · red list
- Last import refusal
- Baked snack food, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Alimentic SAS
12 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalRefused, Baked snack food, n.e.c.NO ENGLISHALLERGENNUTRIT LBLEntry B4Y-0024272-9Source
2022
- Import refusalRefused, BiscuitsLIST INGREALLERGENEntry AMN-0074267-2Source
- Import refusalSource
Refused, 2 lines in one entry: BiscuitsLIST INGRELACKS N/CALLERGENEntry AMN-0075060-0Show 2 linesHide lines
- Refused, BiscuitsLIST INGRELACKS N/CALLERGENEntry AMN-0075060-0Source
- Refused, BiscuitsLIST INGRELACKS N/CALLERGENEntry AMN-0075060-0Source
- Import refusalRefused, BiscuitsLIST INGRELACKS N/CALLERGENEntry AMN-0070386-4Source
- Import refusalRefused, Baked snack food, n.e.c.NO ENGLISHUSUAL NAMEEntry AMN-0067767-0Source
2020
2018
2017
- Import alert listingListed on Import Alert 99-39red listAchiras Huilenses Celio Cheese BiscuitSource
- Import alert listingListed on Import Alert 99-22red listAchiras Huilenses Celio Cheese BiscuitSource
- Import refusalRefused, Plain cookies,biscuits and wafers, n.e.c.NUTRIT LBLEntry N56-0024442-4Source
- Import refusalRefused, Cheese puffs, bakedALLERGENEntry K09-0062134-1Source
Refusal charges, in plain English
- ALLERGEN8 refused lines
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
- LIST INGRE4 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- LACKS N/C3 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NO ENGLISH2 refused lines
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about Alimentic SAS
- Is Alimentic SAS on an FDA import alert?
- Yes. As of October 25, 2026, Alimentic SAS is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for achiras huilenses celio cheese biscuit; FDA published the listing on November 6, 2017.
- Has FDA refused shipments from Alimentic SAS?
- Yes. FDA refused 10 shipment lines from Alimentic SAS between September 14, 2017 and August 3, 2023. The most recent, on August 3, 2023, was baked snack food, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Alimentic SAS's shipments?
- The most frequent charges are ALLERGEN (major food allergen not declared, 8 lines) and LIST INGRE (ingredients not listed, 4 lines).
- What is Alimentic SAS's FEI number?
- Alimentic SAS's FDA Establishment Identifier (FEI) is 3008904124.
- Can shipments from Alimentic SAS still enter the U.S.?
- Shipments of achiras huilenses celio cheese biscuit from Alimentic SAS can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.