Biogo S.A.
FDA import alert and refusal historyWroclaw, PolandFEI 3039086014
Recorded by FDA as BIOGO S.A.
As of October 26, 2026, Biogo S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 12, 2025, most often for required label information not in english (NO ENGLISH).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NO ENGLISH
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Biogo S.A.
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NO ENGLISHEntry 799-3226837-0Source
Refusal charges, in plain English
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
Questions about Biogo S.A.
- Is Biogo S.A. on an FDA import alert?
- No listing for Biogo 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 Poland page.
- Has FDA refused shipments from Biogo S.A.?
- Yes. FDA refused 1 shipment line from Biogo S.A. on November 12, 2025. The most recent, on November 12, 2025, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NO ENGLISH (required label information not in english).
- Why did FDA refuse Biogo S.A.'s shipments?
- The most frequent charge is NO ENGLISH (required label information not in english, 1 line).
- What is Biogo S.A.'s FEI number?
- Biogo S.A.'s FDA Establishment Identifier (FEI) is 3039086014.
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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.