Sri Varu Impex and Logistics

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

Refusal charges, in plain English

• SALMONELLA3 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.

• 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.

• LACKS FIRM1 refused line

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

Questions about Sri Varu Impex and Logistics

Is Sri Varu Impex and Logistics on an FDA import alert?

Yes. As of October 26, 2026, Sri Varu Impex and Logistics is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for dried red chiles; FDA published the listing on March 31, 2025.

Has FDA refused shipments from Sri Varu Impex and Logistics?

Yes. FDA refused 3 shipment lines from Sri Varu Impex and Logistics between March 19, 2025 and June 5, 2025. The most recent, on June 5, 2025, was capsicums (cayenne chili, hot peppers), whole (spice), charged as SALMONELLA (salmonella).

Why did FDA refuse Sri Varu Impex and Logistics's shipments?

The most frequent charges are SALMONELLA (salmonella, 3 lines) and FILTHY (filthy, putrid or decomposed substance, 1 line).

When was Sri Varu Impex and Logistics last inspected by FDA?

FDA's most recent inspection of Sri Varu Impex and Logistics with a final classification is dated August 16, 2018 and was classified NAI (No Action Indicated).

What is Sri Varu Impex and Logistics's FEI number?

Sri Varu Impex and Logistics's FDA Establishment Identifier (FEI) is 3009738884.

Can shipments from Sri Varu Impex and Logistics still enter the U.S.?

Shipments of dried red chiles from Sri Varu Impex and Logistics 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).