Grossman
FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 3007663578
As of October 25, 2026, Grossman is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on February 12, 2026, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin b12 (cyanocobalamin) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grossman
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: Vitamin b12 (cyanocobalamin); Folic acid (vitamin)UNAPPROVEDEntry AEK-9407193-1Show 2 linesHide lines
- Refused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry AEK-9407193-1Source
- Refused, Folic acid (vitamin)UNAPPROVEDEntry AEK-9407193-1Source
Refusal charges, in plain English
- 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.
Questions about Grossman
- Is Grossman on an FDA import alert?
- No listing for Grossman 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 Grossman?
- Yes. FDA refused 2 shipment lines from Grossman on February 12, 2026. The most recent, on February 12, 2026, was vitamin b12 (cyanocobalamin), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Grossman's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Grossman's FEI number?
- Grossman's FDA Establishment Identifier (FEI) is 3007663578.
Buying from Grossman?
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.