Supharma SA Laboratory
FDA import alert and refusal historyGuatemala, GuatemalaFEI 3024559208
Recorded by FDA as SUPHARMA SA LABORATORY
As of October 26, 2026, Supharma SA Laboratory is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 16, 2026, 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
- Ginseng (herbal & botanicals, not teas) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Supharma SA Laboratory
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Ginseng (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-9626498-9Source
Refusal charges, in plain English
- UNAPPROVED1 refused line
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 Supharma SA Laboratory
- Is Supharma SA Laboratory on an FDA import alert?
- No listing for Supharma SA Laboratory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
- Has FDA refused shipments from Supharma SA Laboratory?
- Yes. FDA refused 1 shipment line from Supharma SA Laboratory on September 16, 2026. The most recent, on September 16, 2026, was ginseng (herbal & botanicals, not teas), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Supharma SA Laboratory's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Supharma SA Laboratory's FEI number?
- Supharma SA Laboratory's FDA Establishment Identifier (FEI) is 3024559208.
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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.