Vitactivate
FDA import alert and refusal historyBurnaby, CanadaFEI 3014268303
Recorded by FDA as VITACTIVATE
As of October 25, 2026, Vitactivate is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between January 17, 2019 and January 29, 2019, 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
- Herbals & botanicals (not teas), n.e.c. · DIRECTIONS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vitactivate
3 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalSource
Refused, 2 lines in one entry: Herbals & botanicals (not teas), n.e.c.; Saw palmetto (herbal & botanicals, not teas)DIRECTIONSDIETARYLBLLACKS FIRMNCONTACTEntry SCS-1371979-5Show 2 linesHide lines
- Refused, Herbals & botanicals (not teas), n.e.c.DIRECTIONSDIETARYLBLLACKS FIRMNCONTACTNUTRIT LBLUNAPPROVEDEntry SCS-1371979-5Source
- Refused, Saw palmetto (herbal & botanicals, not teas)DIRECTIONSDIETARYLBLLACKS FIRMNCONTACTNUTRIT LBLUNAPPROVEDEntry SCS-1371979-5Source
- Import refusalRefused, Herbals & botanicals (not teas), n.e.c.LIST INGREDIETARYLBLFALSENCONTACTEntry SCS-2226803-2Source
Refusal charges, in plain English
- DIETARYLBL3 refused lines
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).
- NCONTACT3 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.
- DIRECTIONS2 refused lines
DIRECTIONS
- LACKS FIRM2 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- NUTRIT LBL2 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.
- 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.
- 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).
Questions about Vitactivate
- Is Vitactivate on an FDA import alert?
- No listing for Vitactivate appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Canada page.
- Has FDA refused shipments from Vitactivate?
- Yes. FDA refused 3 shipment lines from Vitactivate between January 17, 2019 and January 29, 2019. The most recent, on January 29, 2019, was herbals & botanicals (not teas), n.e.c., charged as DIRECTIONS (directions).
- Why did FDA refuse Vitactivate's shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 3 lines) and NCONTACT (no u.s. adverse event contact on supplement label, 3 lines).
- What is Vitactivate's FEI number?
- Vitactivate's FDA Establishment Identifier (FEI) is 3014268303.
Buying from Vitactivate?
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.