Pantainorasingh Manufacturer Co., Ltd.

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

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.

• FSVP VIO1 refused line

  Importer not in compliance with FSVP

  The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

• PESTICIDE1 refused line

  Pesticide chemical residue

  The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about Pantainorasingh Manufacturer Co., Ltd.

Is Pantainorasingh Manufacturer Co., Ltd. on an FDA import alert?

Yes. As of October 26, 2026, Pantainorasingh Manufacturer Co., Ltd. is on the green list of FDA Import Alert 16-25, “Processed crabmeat from Thailand”, for crab paste in soybean oil; FDA published the listing on September 18, 2009.

Has FDA refused shipments from Pantainorasingh Manufacturer Co., Ltd.?

Yes. FDA refused 5 shipment lines from Pantainorasingh Manufacturer Co., Ltd. between May 12, 2017 and November 17, 2025. The most recent, on November 17, 2025, was pastes, n.e.c., charged as FILTHY (filthy, putrid or decomposed substance).

Why did FDA refuse Pantainorasingh Manufacturer Co., Ltd.'s shipments?

The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 2 lines) and FSVP VIO (importer not in compliance with fsvp, 1 line).

When was Pantainorasingh Manufacturer Co., Ltd. last inspected by FDA?

FDA's most recent inspection of Pantainorasingh Manufacturer Co., Ltd. with a final classification is dated May 25, 2016 and was classified VAI (Voluntary Action Indicated).

What is Pantainorasingh Manufacturer Co., Ltd.'s FEI number?

Pantainorasingh Manufacturer Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004691124.