Bakbel Europe SA
FDA import alert and refusal historySeneffe, BelgiumFEI 3008585519
As of October 26, 2026, Bakbel Europe SA has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 9, 2016, was classified VAI (Voluntary Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Bakbel Europe SA
2 records, newest first. Each line links to the FDA page it came from.
Questions about Bakbel Europe SA
- Is Bakbel Europe SA on an FDA import alert?
- No listing for Bakbel Europe SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Belgium page.
- Has FDA refused shipments from Bakbel Europe SA?
- No FDA import refusals for Bakbel Europe SA appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Bakbel Europe SA last inspected by FDA?
- FDA's most recent inspection of Bakbel Europe SA with a final classification is dated December 9, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Bakbel Europe SA's FEI number?
- Bakbel Europe SA's FDA Establishment Identifier (FEI) is 3008585519.
Buying from Bakbel Europe SA?
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.