Intergrow Brands Private Limited
FDA import alert and refusal historyErnakulam, IndiaFEI 3043838902
Recorded by FDA as INTERGROW BRANDS PRIVATE LIMITED
As of October 26, 2026, Intergrow Brands Private Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on July 31, 2026, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tamarind, dried or paste · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Intergrow Brands Private Limited
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY2 refused lines
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.
Questions about Intergrow Brands Private Limited
- Is Intergrow Brands Private Limited on an FDA import alert?
- No listing for Intergrow Brands Private Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Intergrow Brands Private Limited?
- Yes. FDA refused 2 shipment lines from Intergrow Brands Private Limited on July 31, 2026. The most recent, on July 31, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Intergrow Brands Private Limited's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Intergrow Brands Private Limited's FEI number?
- Intergrow Brands Private Limited's FDA Establishment Identifier (FEI) is 3043838902.
Buying from Intergrow Brands Private Limited?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.