Penver Products Limited

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

Refusal charges, in plain English

• VETDRUGRES4 refused lines

  Animal drug residue

  The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.

• LACKS FIRM3 refused lines

  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.

• SALMONELLA1 refused line

  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 Penver Products Limited

Is Penver Products Limited on an FDA import alert?

Yes. As of October 26, 2026, Penver Products Limited is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; cooked shrimp; FDA published the listing on August 30, 2019.

Has FDA refused shipments from Penver Products Limited?

Yes. FDA refused 5 shipment lines from Penver Products Limited between April 30, 2019 and August 5, 2024. The most recent, on August 5, 2024, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as VETDRUGRES (animal drug residue).

Why did FDA refuse Penver Products Limited's shipments?

The most frequent charges are VETDRUGRES (animal drug residue, 4 lines) and LACKS FIRM (manufacturer name and address missing, 3 lines).

When was Penver Products Limited last inspected by FDA?

FDA's most recent inspection of Penver Products Limited with a final classification is dated September 12, 2019 and was classified NAI (No Action Indicated).

What is Penver Products Limited's FEI number?

Penver Products Limited's FDA Establishment Identifier (FEI) is 3011572567.