Piersan Centroamericano
FDA import alert and refusal historyGuatemala City, GuatemalaFEI 3031057878
Recorded by FDA as PIERSAN CENTROAMERICANO
As of October 26, 2026, Piersan Centroamericano is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between December 9, 2025 and July 20, 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
- Vitamin, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Piersan Centroamericano
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vitamin, n.e.c.UNAPPROVEDEntry 1FX-6292500-3Source
2025
- Import refusalRefused, Vitamin b1 (thiamine)UNAPPROVEDEntry 799-1723798-7Source
Refusal charges, in plain English
- UNAPPROVED2 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 Piersan Centroamericano
- Is Piersan Centroamericano on an FDA import alert?
- No listing for Piersan Centroamericano 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 Piersan Centroamericano?
- Yes. FDA refused 2 shipment lines from Piersan Centroamericano between December 9, 2025 and July 20, 2026. The most recent, on July 20, 2026, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Piersan Centroamericano's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Piersan Centroamericano's FEI number?
- Piersan Centroamericano's FDA Establishment Identifier (FEI) is 3031057878.
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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.