Develey Senf&Feinkost GmbH
FDA import alert and refusal historyUnterhaching, GermanyFEI 3004406391
As of October 26, 2026, Develey Senf&Feinkost GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on May 4, 2017, most often for nutrition information missing from label (NUTRIT LBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Mustard, prepared · NUTRIT LBL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Develey Senf&Feinkost GmbH
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 2 lines in one entry: Mustard, preparedNUTRIT LBLEntry U52-7720994-1Show 2 linesHide lines
- Refused, Mustard, preparedNUTRIT LBLEntry U52-7720994-1Source
- Refused, Mustard, preparedNUTRIT LBLEntry U52-7720994-1Source
Refusal charges, in plain English
- NUTRIT LBL2 refused lines
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 Develey Senf&Feinkost GmbH
- Is Develey Senf&Feinkost GmbH on an FDA import alert?
- No listing for Develey Senf&Feinkost GmbH 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 Develey Senf&Feinkost GmbH?
- Yes. FDA refused 2 shipment lines from Develey Senf&Feinkost GmbH on May 4, 2017. The most recent, on May 4, 2017, was mustard, prepared, charged as NUTRIT LBL (nutrition information missing from label).
- Why did FDA refuse Develey Senf&Feinkost GmbH's shipments?
- The most frequent charge is NUTRIT LBL (nutrition information missing from label, 2 lines).
- What is Develey Senf&Feinkost GmbH's FEI number?
- Develey Senf&Feinkost GmbH's FDA Establishment Identifier (FEI) is 3004406391.
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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.