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Laboratoire Gallia-Bsa

FDA import alert and refusal historyLimonest, FranceFEI 3043886924

Recorded by FDA as LABORATOIRE GALLIA-BSA

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Example subjectLaboratoire Gallia-Bs added to Import Alert 16-129 (red list)

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As of October 26, 2026, Laboratoire Gallia-Bsa is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on August 20, 2026, 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
Milk base infant formula product (0-12 months), powder formula · FALSE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Laboratoire Gallia-Bsa

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

2026

  1. Import refusal
    Refused, Milk base infant formula product (0-12 months), powder formulaFALSEEntry SCS-0774372-4
    Source

Refusal charges, in plain English

  • FALSE1 refused line

    False or misleading labeling

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

Questions about Laboratoire Gallia-Bsa

Is Laboratoire Gallia-Bsa on an FDA import alert?
No listing for Laboratoire Gallia-Bsa appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Laboratoire Gallia-Bsa?
Yes. FDA refused 1 shipment line from Laboratoire Gallia-Bsa on August 20, 2026. The most recent, on August 20, 2026, was milk base infant formula product (0-12 months), powder formula, charged as FALSE (false or misleading labeling).
Why did FDA refuse Laboratoire Gallia-Bsa's shipments?
The most frequent charge is FALSE (false or misleading labeling, 1 line).
What is Laboratoire Gallia-Bsa's FEI number?
Laboratoire Gallia-Bsa's FDA Establishment Identifier (FEI) is 3043886924.

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Example subjectLaboratoire Gallia-Bs 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.