Laboratorios Ancalmo
FDA import alert and refusal historyAntiguo Cuscatlan, El SalvadorFEI 3015192151
Recorded by FDA as LABORATORIOS ANCALMO
As of October 26, 2026, Laboratorios Ancalmo is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 7, 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
- Vitamin e (tocopherol) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Laboratorios Ancalmo
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Vitamin e (tocopherol)UNAPPROVEDEntry AEK-8207888-0Source
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 Ancalmo
- Is Laboratorios Ancalmo on an FDA import alert?
- No listing for Laboratorios Ancalmo appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.
- Has FDA refused shipments from Laboratorios Ancalmo?
- Yes. FDA refused 1 shipment line from Laboratorios Ancalmo on February 7, 2025. The most recent, on February 7, 2025, was vitamin e (tocopherol), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Laboratorios Ancalmo's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Laboratorios Ancalmo's FEI number?
- Laboratorios Ancalmo's FDA Establishment Identifier (FEI) is 3015192151.
Buying from Laboratorios Ancalmo?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.