Guruji Products Private
FDA import alert and refusal historyIndore, IndiaFEI 3045571743
Recorded by FDA as GURUJI PRODUCTS PRIVATE
As of October 26, 2026, Guruji Products Private is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 24, 2026, most often for color additive unsafe under section 721 (UNSAFE COL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Beverage base not mentioned elsewhere, n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Guruji Products Private
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Beverage base not mentioned elsewhere, n.e.c.UNSAFE COLEntry H77-0241555-2Source
Refusal charges, in plain English
- 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 Guruji Products Private
- Is Guruji Products Private on an FDA import alert?
- No listing for Guruji Products Private 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 Guruji Products Private?
- Yes. FDA refused 1 shipment line from Guruji Products Private on September 24, 2026. The most recent, on September 24, 2026, was beverage base not mentioned elsewhere, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Guruji Products Private's shipments?
- The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
- What is Guruji Products Private's FEI number?
- Guruji Products Private's FDA Establishment Identifier (FEI) is 3045571743.
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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.