Similasan AG
FDA import alert and refusal historyJonen, SwitzerlandFEI 1000110034
As of October 26, 2026, Similasan AG is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 23, 2026, most often for drug gmps (DRUG GMPS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, n.e.c. · DRUG GMPS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Similasan AG
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- DRUG GMPS1 refused line
DRUG GMPS
Questions about Similasan AG
- Is Similasan AG on an FDA import alert?
- No listing for Similasan AG appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Switzerland page.
- Has FDA refused shipments from Similasan AG?
- Yes. FDA refused 1 shipment line from Similasan AG on February 23, 2026. The most recent, on February 23, 2026, was vitamin, n.e.c., charged as DRUG GMPS (drug gmps).
- Why did FDA refuse Similasan AG's shipments?
- The most frequent charge is DRUG GMPS (drug gmps, 1 line).
- What is Similasan AG's FEI number?
- Similasan AG's FDA Establishment Identifier (FEI) is 1000110034.
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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.