Unilever Deutschland Produktions GmbH & Co. OHG
FDA import alert and refusal historyHeilbronn, GermanyFEI 3009909443
As of October 26, 2026, Unilever Deutschland Produktions GmbH & Co. OHG is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 12, 2019, most often for net quantity statement missing (LACKS N/C).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Sauces, n.e.c. · LACKS N/C
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Unilever Deutschland Produktions GmbH & Co. OHG
2 records, newest first. Each line links to the FDA page it came from.
2026
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2019
- Import refusalRefused, Sauces, n.e.c.LACKS N/CNUTRIT LBLNO PROCESSEntry AGW-5520906-6Source
Refusal charges, in plain English
- 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 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.
Questions about Unilever Deutschland Produktions GmbH & Co. OHG
- Is Unilever Deutschland Produktions GmbH & Co. OHG on an FDA import alert?
- No listing for Unilever Deutschland Produktions GmbH & Co. OHG appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
- Has FDA refused shipments from Unilever Deutschland Produktions GmbH & Co. OHG?
- Yes. FDA refused 1 shipment line from Unilever Deutschland Produktions GmbH & Co. OHG on February 12, 2019. The most recent, on February 12, 2019, was sauces, n.e.c., charged as LACKS N/C (net quantity statement missing).
- Why did FDA refuse Unilever Deutschland Produktions GmbH & Co. OHG's shipments?
- The most frequent charges are LACKS N/C (net quantity statement missing, 1 line) and NO PROCESS (no scheduled process filed, 1 line).
- When was Unilever Deutschland Produktions GmbH & Co. OHG last inspected by FDA?
- FDA's most recent inspection of Unilever Deutschland Produktions GmbH & Co. OHG with a final classification is dated April 8, 2026 and was classified NAI (No Action Indicated).
- What is Unilever Deutschland Produktions GmbH & Co. OHG's FEI number?
- Unilever Deutschland Produktions GmbH & Co. OHG's FDA Establishment Identifier (FEI) is 3009909443.
Buying from Unilever Deutschland Produktions GmbH & Co. OHG?
Watch it and get the FDA record the day it changes. Free for one supplier.
SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.