Alexfarma
FDA import alert and refusal historyGoiania, BrazilFEI 3040940934
Recorded by FDA as ALEXFARMA
As of October 25, 2026, Alexfarma is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines on November 17, 2025, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Ashwagandha (herbal & botanicals, not teas) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Alexfarma
6 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 6 lines in one entry: Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Show 6 linesHide lines
- Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Source
- Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Source
- Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Source
- Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Source
- Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Source
- Refused, Ashwagandha (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-7927387-4Source
Refusal charges, in plain English
- UNAPPROVED6 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Alexfarma
- Is Alexfarma on an FDA import alert?
- No listing for Alexfarma appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Brazil page.
- Has FDA refused shipments from Alexfarma?
- Yes. FDA refused 6 shipment lines from Alexfarma on November 17, 2025. The most recent, on November 17, 2025, was ashwagandha (herbal & botanicals, not teas), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Alexfarma's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 6 lines).
- What is Alexfarma's FEI number?
- Alexfarma's FDA Establishment Identifier (FEI) is 3040940934.
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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.