Neeli Aqua Private Limited

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

Refusal charges, in plain English

• NITROFURAN3 refused lines

  Nitrofurans

  The product appeared to contain nitrofurans, a class of antibiotic drugs, which are treated as an unsafe food additive under section 409 of the FD&C Act.

• VETDRUGRES3 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.

• INSANITARY1 refused line

  Prepared, packed or held under insanitary conditions

  The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.

Questions about Neeli Aqua Private Limited

Is Neeli Aqua Private Limited on an FDA import alert?

Yes. As of October 26, 2026, Neeli Aqua Private Limited is on the green list of FDA Import Alert 16-35, “Raw and cooked shrimp from India”, for raw shrimp; FDA published the listing on July 1, 2016.

Has FDA refused shipments from Neeli Aqua Private Limited?

Yes. FDA refused 4 shipment lines from Neeli Aqua Private Limited between April 7, 2020 and October 2, 2026. The most recent, on October 2, 2026, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as INSANITARY (prepared, packed or held under insanitary conditions).

Why did FDA refuse Neeli Aqua Private Limited's shipments?

The most frequent charges are NITROFURAN (nitrofurans, 3 lines) and VETDRUGRES (animal drug residue, 3 lines).

When was Neeli Aqua Private Limited last inspected by FDA?

FDA's most recent inspection of Neeli Aqua Private Limited with a final classification is dated June 11, 2019 and was classified NAI (No Action Indicated).

What is Neeli Aqua Private Limited's FEI number?

Neeli Aqua Private Limited's FDA Establishment Identifier (FEI) is 3013316507.