Ganpati Scientifics

11 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• SALMONELLA9 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.

• FILTHY6 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.

• FOREIGN OB6 refused lines

  FOREIGN OB

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• UNSAFE ADD1 refused line

  Food additive unsafe under section 409

  The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Ganpati Scientifics

Is Ganpati Scientifics on an FDA import alert?

Yes. As of October 25, 2026, Ganpati Scientifics is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for quinoa; FDA published the listing on January 19, 2022.

Has FDA refused shipments from Ganpati Scientifics?

Yes. FDA refused 10 shipment lines from Ganpati Scientifics between December 29, 2021 and February 25, 2025. The most recent, on February 25, 2025, was pepper, black, ground, cracked (spice), charged as SALMONELLA (salmonella).

Why did FDA refuse Ganpati Scientifics's shipments?

The most frequent charges are SALMONELLA (salmonella, 9 lines) and FILTHY (filthy, putrid or decomposed substance, 6 lines).

What is Ganpati Scientifics's FEI number?

Ganpati Scientifics's FDA Establishment Identifier (FEI) is 3017150170.

Can shipments from Ganpati Scientifics still enter the U.S.?

Shipments of quinoa from Ganpati Scientifics can be detained without physical examination under Import Alert 99-19; 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).