Pudliszki Sp. z o.o.

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

Refusal charges, in plain English

• 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.

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• NO ENGLISH1 refused line

  Required label information not in English

  Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

• 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.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

• STD IDENT1 refused line

  Does not conform to standard of identity

  The product appeared to be represented as a food that has an FDA standard of identity, but not to conform to that standard.

Questions about Pudliszki Sp. z o.o.

Is Pudliszki Sp. z o.o. on an FDA import alert?

No listing for Pudliszki Sp. z o.o. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.

Has FDA refused shipments from Pudliszki Sp. z o.o.?

Yes. FDA refused 1 shipment line from Pudliszki Sp. z o.o. on January 23, 2020. The most recent, on January 23, 2020, was peas, bean and pea sprouts, charged as STD IDENT (does not conform to standard of identity).

Why did FDA refuse Pudliszki Sp. z o.o.'s shipments?

The most frequent charges are LACKS FIRM (manufacturer name and address missing, 1 line) and LACKS N/C (net quantity statement missing, 1 line).

When was Pudliszki Sp. z o.o. last inspected by FDA?

FDA's most recent inspection of Pudliszki Sp. z o.o. with a final classification is dated September 18, 2024 and was classified VAI (Voluntary Action Indicated).

What is Pudliszki Sp. z o.o.'s FEI number?

Pudliszki Sp. z o.o.'s FDA Establishment Identifier (FEI) is 3014827515.