Acenzia Inc.

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

Refusal charges, in plain English

• UNAPPROVED7 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.

• DIETARYLBL2 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).

• 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.

• FRNMFGREG1 refused line

  FRNMFGREG

• MFR INSAN1 refused line

  Insanitary manufacturing, processing or packing

  The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

• NOT LISTED1 refused line

  Product not listed with FDA

  The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.

Questions about Acenzia Inc.

Is Acenzia Inc. on an FDA import alert?

No listing for Acenzia Inc. 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 Acenzia Inc.?

Yes. FDA refused 10 shipment lines from Acenzia Inc. between December 18, 2019 and September 16, 2026. The most recent, on September 16, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as DIETARYLBL (not identified as a dietary supplement).

Why did FDA refuse Acenzia Inc.'s shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 7 lines) and DIETARYLBL (not identified as a dietary supplement, 2 lines).

When was Acenzia Inc. last inspected by FDA?

FDA's most recent inspection of Acenzia Inc. with a final classification is dated August 22, 2024 and was classified NAI (No Action Indicated).

What is Acenzia Inc.'s FEI number?

Acenzia Inc.'s FDA Establishment Identifier (FEI) is 3008764049.