IPOSEA S.r.l.

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

Refusal charges, in plain English

• 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.

• USUAL NAME1 refused line

  Common or usual name missing

  The label appeared not to show the common or usual name of the food.

Questions about IPOSEA S.r.l.

Is IPOSEA S.r.l. on an FDA import alert?

No listing for IPOSEA S.r.l. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Italy page.

Has FDA refused shipments from IPOSEA S.r.l.?

Yes. FDA refused 2 shipment lines from IPOSEA S.r.l. between August 12, 2022 and January 6, 2023. The most recent, on January 6, 2023, was mixed vegetables, with sauce, n.e.c., charged as NO PROCESS (no scheduled process filed).

Why did FDA refuse IPOSEA S.r.l.'s shipments?

The most frequent charges are NO PROCESS (no scheduled process filed, 1 line) and NUTRIT LBL (nutrition information missing from label, 1 line).

When was IPOSEA S.r.l. last inspected by FDA?

FDA's most recent inspection of IPOSEA S.r.l. with a final classification is dated September 16, 2024 and was classified NAI (No Action Indicated).

What is IPOSEA S.r.l.'s FEI number?

IPOSEA S.r.l.'s FDA Establishment Identifier (FEI) is 3004270814.