Honeymax S.A.
FDA import alert and refusal historyCiudad Autonoma Buenos Aires, ArgentinaFEI 3005144041
As of October 26, 2026, Honeymax S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on January 26, 2024, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Honeymax S.A.
2 records, newest first. Each line links to the FDA page it came from.
Questions about Honeymax S.A.
- Is Honeymax S.A. on an FDA import alert?
- No listing for Honeymax 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 Argentina page.
- Has FDA refused shipments from Honeymax S.A.?
- No FDA import refusals for Honeymax S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Honeymax S.A. last inspected by FDA?
- FDA's most recent inspection of Honeymax S.A. with a final classification is dated January 26, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Honeymax S.A.'s FEI number?
- Honeymax S.A.'s FDA Establishment Identifier (FEI) is 3005144041.
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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.