Annai Enterprises
FDA import alert and refusal historyChennai, IndiaFEI 3010219965
Recorded by FDA as ANNAI ENTERPRISES
As of October 26, 2026, Annai Enterprises (Chennai, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for gold finger dried wafers, published by FDA on February 19, 2013, and has 2 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
- Rice, basmati, processed (packaged) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Annai Enterprises
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Annai Enterprises
- Is Annai Enterprises on an FDA import alert?
- Yes. As of October 26, 2026, Annai Enterprises is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for gold finger dried wafers; FDA published the listing on February 19, 2013.
- Has FDA refused shipments from Annai Enterprises?
- Yes. FDA refused 2 shipment lines from Annai Enterprises between August 16, 2017 and December 1, 2023. The most recent, on December 1, 2023, was rice, basmati, processed (packaged), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Annai Enterprises's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and PESTICIDE (pesticide chemical residue, 1 line).
- What is Annai Enterprises's FEI number?
- Annai Enterprises's FDA Establishment Identifier (FEI) is 3010219965.
- Can shipments from Annai Enterprises still enter the U.S.?
- Shipments of gold finger dried wafers from Annai Enterprises 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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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.