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Remitente Laboratorios Ordesa S.L.

FDA import alert and refusal historyBarcelonabarcelona, SpainFEI 3010171863

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Example subjectRemitente Laboratorios Ordesa S.L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Remitente Laboratorios Ordesa S.L. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 16, 2023, most often for lack notif (LACK NOTIF).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Milk base infant formula product (0-12 months), powder formula · LACK NOTIF
Last warning letter
None found
Last inspection
None on record

Every FDA record for Remitente Laboratorios Ordesa S.L.

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

2023

  1. Import refusal
    Refused, Milk base infant formula product (0-12 months), powder formulaLACK NOTIFEntry K51-0101024-4
    Source

Refusal charges, in plain English

Questions about Remitente Laboratorios Ordesa S.L.

Is Remitente Laboratorios Ordesa S.L. on an FDA import alert?
No listing for Remitente Laboratorios Ordesa S.L. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
Has FDA refused shipments from Remitente Laboratorios Ordesa S.L.?
Yes. FDA refused 1 shipment line from Remitente Laboratorios Ordesa S.L. on February 16, 2023. The most recent, on February 16, 2023, was milk base infant formula product (0-12 months), powder formula, charged as LACK NOTIF (lack notif).
Why did FDA refuse Remitente Laboratorios Ordesa S.L.'s shipments?
The most frequent charge is LACK NOTIF (lack notif, 1 line).
What is Remitente Laboratorios Ordesa S.L.'s FEI number?
Remitente Laboratorios Ordesa S.L.'s FDA Establishment Identifier (FEI) is 3010171863.

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Example subjectRemitente Laboratorios Ordesa S.L added to Import Alert 16-129 (red list)

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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.