Ghi Engitech Mark
FDA import alert and refusal historyVadodara, IndiaFEI 3038356030
Recorded by FDA as GHI ENGITECH MARK
As of October 25, 2026, Ghi Engitech Mark is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on March 10, 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
- Pepper, black, ground, cracked (spice) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ghi Engitech Mark
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: Pepper, black, ground, cracked (spice)FILTHYSALMONELLAEntry SCS-1489099-6Show 2 linesHide lines
- Refused, Pepper, black, ground, cracked (spice)FILTHYSALMONELLAEntry SCS-1489099-6Source
- Refused, Pepper, black, ground, cracked (spice)FILTHYSALMONELLAEntry SCS-1489099-6Source
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.
- SALMONELLA2 refused lines
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Ghi Engitech Mark
- Is Ghi Engitech Mark on an FDA import alert?
- No listing for Ghi Engitech Mark appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Ghi Engitech Mark?
- Yes. FDA refused 2 shipment lines from Ghi Engitech Mark on March 10, 2026. The most recent, on March 10, 2026, was pepper, black, ground, cracked (spice), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Ghi Engitech Mark's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 2 lines) and SALMONELLA (salmonella, 2 lines).
- What is Ghi Engitech Mark's FEI number?
- Ghi Engitech Mark's FDA Establishment Identifier (FEI) is 3038356030.
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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.