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Orbe, S.A.

FDA import alert and refusal historyVigo, SpainFEI 3013022970

Recorded by FDA as ORBE, S.A.

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Example subjectOrbe, S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Orbe, S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines between May 2, 2017 and May 15, 2017, most often for false or misleading labeling (FALSE).

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

Current status

Import alerts
Not listed
Last import refusal
Octopus, other aquatic species · FALSE
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Orbe, S.A.

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

2019

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2017

  1. Import refusal
    Refused, Octopus, other aquatic speciesFALSEEntry 438-0040293-5
    Source
  2. Import refusal
    Refused, 2 lines in one entry: Octopus, other aquatic speciesFALSEEntry 256-0347144-9Show 2 lines
    • Refused, Octopus, other aquatic speciesFALSEEntry 256-0347144-9Source
    • Refused, Octopus, other aquatic speciesFALSEEntry 256-0347144-9Source
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Octopus, other aquatic speciesWRONG IDENEntry 256-0347145-6Show 2 lines
    Source
  4. Import refusal
    Refused, Octopus, other aquatic speciesFALSEEntry 256-0347144-9
    Source
  5. Import refusal
    Refused, Octopus, other aquatic speciesWRONG IDENEntry 256-0347145-6
    Source

2011

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • FALSE4 refused lines

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • WRONG IDEN3 refused lines

    WRONG IDEN

Questions about Orbe, S.A.

Is Orbe, S.A. on an FDA import alert?
No listing for Orbe, S.A. 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 Orbe, S.A.?
Yes. FDA refused 7 shipment lines from Orbe, S.A. between May 2, 2017 and May 15, 2017. The most recent, on May 15, 2017, was octopus, other aquatic species, charged as FALSE (false or misleading labeling).
Why did FDA refuse Orbe, S.A.'s shipments?
The most frequent charges are FALSE (false or misleading labeling, 4 lines) and WRONG IDEN (wrong iden, 3 lines).
When was Orbe, S.A. last inspected by FDA?
FDA's most recent inspection of Orbe, S.A. with a final classification is dated December 19, 2019 and was classified NAI (No Action Indicated).
What is Orbe, S.A.'s FEI number?
Orbe, S.A.'s FDA Establishment Identifier (FEI) is 3013022970.

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Example subjectOrbe, S.A 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.