Vanity Vision

12 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• SUPPL GMP5 refused lines

  Dietary supplement CGMP not met

  The product appeared to be a dietary supplement prepared, packed, or held under conditions that do not meet current good manufacturing practice (CGMP) regulations.

• FALSE2 refused lines

  False or misleading labeling

  The labeling appeared to be false or misleading in some particular.

• 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.

• INCONSPICU1 refused line

  Required information not conspicuous

  Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

• 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.

• VITAMN LBL1 refused line

  VITAMN LBL

Questions about Vanity Vision

Is Vanity Vision on an FDA import alert?

Yes. As of October 26, 2026, Vanity Vision is on the red list of FDA Import Alert 54-14, “Supplements from firms not meeting supplement GMP”, for all dietary supplement products; FDA published the listing on April 15, 2026.

Has FDA refused shipments from Vanity Vision?

Yes. FDA refused 9 shipment lines from Vanity Vision between September 27, 2024 and September 20, 2026. The most recent, on September 20, 2026, was dietary conventional foods, n.e.c., charged as SUPPL GMP (dietary supplement cgmp not met).

Why did FDA refuse Vanity Vision's shipments?

The most frequent charges are SUPPL GMP (dietary supplement cgmp not met, 5 lines) and FALSE (false or misleading labeling, 2 lines).

When was Vanity Vision last inspected by FDA?

FDA's most recent inspection of Vanity Vision with a final classification is dated November 19, 2025 and was classified OAI (Official Action Indicated).

What is Vanity Vision's FEI number?

Vanity Vision's FDA Establishment Identifier (FEI) is 3027445987.

Can shipments from Vanity Vision still enter the U.S.?

Shipments of all dietary supplement products from Vanity Vision can be detained without physical examination under Import Alert 54-14; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).