Laboratorios Grossman S.A

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

Refusal charges, in plain English

• UNAPPROVED5 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.

• NOT LISTED2 refused lines

  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 Laboratorios Grossman S.A

Is Laboratorios Grossman S.A on an FDA import alert?

No listing for Laboratorios Grossman S.A appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Mexico page.

Has FDA refused shipments from Laboratorios Grossman S.A?

Yes. FDA refused 5 shipment lines from Laboratorios Grossman S.A between September 11, 2019 and August 3, 2026. The most recent, on August 3, 2026, was multiple vitamins (mvi-12 vitamin combo) (vitamin), charged as NOT LISTED (product not listed with fda).

Why did FDA refuse Laboratorios Grossman S.A's shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 5 lines) and NOT LISTED (product not listed with fda, 2 lines).

What is Laboratorios Grossman S.A's FEI number?

Laboratorios Grossman S.A's FDA Establishment Identifier (FEI) is 3012845835.