Grisi Hnos, S.A. de C.V.
FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 1000424274
As of October 26, 2026, Grisi Hnos, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 15, 2021 and January 8, 2025, 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 c (ascorbic acid) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grisi Hnos, S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Vitamin c (ascorbic acid)UNAPPROVEDEntry 799-4812517-5Source
2021
- Import refusalRefused, Vitamin c (ascorbic acid)UNAPPROVEDEntry 799-1326302-5Source
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 Grisi Hnos, S.A. de C.V.
- Is Grisi Hnos, S.A. de C.V. on an FDA import alert?
- No listing for Grisi Hnos, S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Grisi Hnos, S.A. de C.V.?
- Yes. FDA refused 2 shipment lines from Grisi Hnos, S.A. de C.V. between March 15, 2021 and January 8, 2025. The most recent, on January 8, 2025, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Grisi Hnos, S.A. de C.V.'s shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Grisi Hnos, S.A. de C.V.'s FEI number?
- Grisi Hnos, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 1000424274.
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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.