Peck'S Anchovette

1 record, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• NEEDS FCE1 refused line

  Processor not registered for canned or acidified foods

  The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

• 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.

• UNSAFE COL1 refused line

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Peck'S Anchovette

Is Peck'S Anchovette on an FDA import alert?

No listing for Peck'S Anchovette appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.

Has FDA refused shipments from Peck'S Anchovette?

Yes. FDA refused 1 shipment line from Peck'S Anchovette on February 27, 2018. The most recent, on February 27, 2018, was fish paste, fishery products, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Peck'S Anchovette's shipments?

The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 1 line) and NO PROCESS (no scheduled process filed, 1 line).

What is Peck'S Anchovette's FEI number?

Peck'S Anchovette's FDA Establishment Identifier (FEI) is 3013977015.