Madam Agro-Food Industries
FDA import alert and refusal historyPalghar, IndiaFEI 3013327169
As of October 26, 2026, Madam Agro-Food Industries (Palghar, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for good day nuts cookie; gd badam biscuits, published by FDA on August 7, 2018, and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- Snack foods not elsewhere mentioned, n.e.c. · MFR INSAN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Madam Agro-Food Industries
7 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 3 lines in one entry: Snack foods not elsewhere mentioned, n.e.c.; Rice flakes,puffs,krispies,loops ready to eatMFR INSANMFR INJEntry KM6-3664109-4Show 3 linesHide lines
2018
- Import alert listingListed on Import Alert 45-02red listGood Day Nuts Cookie; GD Badam BiscuitsSource
- Import refusalSource
Refused, 2 lines in one entry: Plain cookies,biscuits and wafers, n.e.c.UNSAFE COLLIST INGREEntry KM6-3514403-3Show 2 linesHide lines
- Refused, Plain cookies,biscuits and wafers, n.e.c.UNSAFE COLEntry KM6-3514403-3Source
- Refused, Plain cookies,biscuits and wafers, n.e.c.LIST INGREEntry KM6-3514403-3Source
- Import refusalRefused, Plain cookies,biscuits and wafers, n.e.c.LABELINGNUTRIT LBLEntry KM6-3512361-5Source
Refusal charges, in plain English
- MFR INJ3 refused lines
Insanitary conditions, may be injurious
The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
- MFR INSAN3 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
- LIST INGRE1 refused line
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).
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Madam Agro-Food Industries
- Is Madam Agro-Food Industries on an FDA import alert?
- Yes. As of October 26, 2026, Madam Agro-Food Industries is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for good day nuts cookie; gd badam biscuits; FDA published the listing on August 7, 2018.
- Has FDA refused shipments from Madam Agro-Food Industries?
- Yes. FDA refused 6 shipment lines from Madam Agro-Food Industries between June 20, 2018 and October 3, 2025. The most recent, on October 3, 2025, was snack foods not elsewhere mentioned, n.e.c., charged as MFR INSAN (insanitary manufacturing, processing or packing).
- Why did FDA refuse Madam Agro-Food Industries's shipments?
- The most frequent charges are MFR INJ (insanitary conditions, may be injurious, 3 lines) and MFR INSAN (insanitary manufacturing, processing or packing, 3 lines).
- What is Madam Agro-Food Industries's FEI number?
- Madam Agro-Food Industries's FDA Establishment Identifier (FEI) is 3013327169.
- Can shipments from Madam Agro-Food Industries still enter the U.S.?
- Shipments of good day nuts cookie; gd badam biscuits from Madam Agro-Food Industries can be detained without physical examination under Import Alert 45-02; 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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