Aphrodite 3D
FDA import alert and refusal historyLuxemburg, LuxembourgFEI 3017652186
Recorded by FDA as APHRODITE 3D
As of October 26, 2026, Aphrodite 3D is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 4, 2021, most often for not identified as a dietary supplement (DIETARYLBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Aphrodite 3D
1 record, newest first. Each line links to the FDA page it came from.
2021
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.LIST INGREDIETARYLBLFALSENCONTACTNUTRIT LBLUNAPPROVEDEntry SCS-3370936-3Source
Refusal charges, in plain English
- 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).
- NCONTACT1 refused line
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 LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- 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 Aphrodite 3D
- Is Aphrodite 3D on an FDA import alert?
- No listing for Aphrodite 3D appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Luxembourg page.
- Has FDA refused shipments from Aphrodite 3D?
- Yes. FDA refused 1 shipment line from Aphrodite 3D on January 4, 2021. The most recent, on January 4, 2021, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Aphrodite 3D's shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 1 line) and FALSE (false or misleading labeling, 1 line).
- What is Aphrodite 3D's FEI number?
- Aphrodite 3D's FDA Establishment Identifier (FEI) is 3017652186.
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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.