Laboratorios Ceguel SA
FDA import alert and refusal historyManagua, NicaraguaFEI 3031822755
Recorded by FDA as LABORATORIOS CEGUEL SA
As of October 26, 2026, Laboratorios Ceguel SA is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 23, 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
- Aloe (herbal and botanical (not teas) ii (continued)) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Laboratorios Ceguel SA
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Aloe (herbal and botanical (not teas) ii (continued))UNAPPROVEDEntry AEK-7601898-3Source
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 Laboratorios Ceguel SA
- Is Laboratorios Ceguel SA on an FDA import alert?
- No listing for Laboratorios Ceguel SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Nicaragua page.
- Has FDA refused shipments from Laboratorios Ceguel SA?
- Yes. FDA refused 1 shipment line from Laboratorios Ceguel SA on September 23, 2025. The most recent, on September 23, 2025, was aloe (herbal and botanical (not teas) ii (continued)), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Laboratorios Ceguel SA's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Laboratorios Ceguel SA's FEI number?
- Laboratorios Ceguel SA's FDA Establishment Identifier (FEI) is 3031822755.
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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.