Hedelab SA
FDA import alert and refusal historyGhlin, BelgiumFEI 3015878588
Recorded by FDA as HEDELAB SA
As of October 26, 2026, Hedelab SA is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on November 12, 2019, most often for no u.s. adverse event contact on supplement label (NCONTACT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · FALSE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hedelab SA
4 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalSource
Refused, 4 lines in one entry: Herbals & botanicals (not teas), n.e.c.FALSENCONTACTNUTRIT LBLDIETARYLBLEntry SCS-7207818-2Show 4 linesHide lines
- Refused, Herbals & botanicals (not teas), n.e.c.FALSENCONTACTNUTRIT LBLEntry SCS-7207818-2Source
- Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTNUTRIT LBLEntry SCS-7207818-2Source
- Refused, Herbals & botanicals (not teas), n.e.c.DIETARYLBLNO ENGLISHNCONTACTNUTRIT LBLEntry SCS-7207818-2Source
- Refused, Herbals & botanicals (not teas), n.e.c.LIST INGREDIETARYINGPLANT PARTNCONTACTEntry SCS-7207818-2Source
Refusal charges, in plain English
- NCONTACT4 refused lines
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- NUTRIT LBL3 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- DIETARYING1 refused line
Dietary ingredients not listed
The dietary supplement label appeared not to list each dietary ingredient and its quantity, or the total quantity of a proprietary blend.
- DIETARYLBL1 refused line
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- NO ENGLISH1 refused line
Required label information not in English
Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.
- PLANT PART1 refused line
PLANT PART
Questions about Hedelab SA
- Is Hedelab SA on an FDA import alert?
- No listing for Hedelab 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 Hedelab SA?
- Yes. FDA refused 4 shipment lines from Hedelab SA on November 12, 2019. The most recent, on November 12, 2019, was herbals & botanicals (not teas), n.e.c., charged as FALSE (false or misleading labeling).
- Why did FDA refuse Hedelab SA's shipments?
- The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 4 lines) and NUTRIT LBL (nutrition information missing from label, 3 lines).
- What is Hedelab SA's FEI number?
- Hedelab SA's FDA Establishment Identifier (FEI) is 3015878588.
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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.