Sabormex, SAPI de C.V.
FDA import alert and refusal historyHeroica Puebla De Zaragoza, MexicoFEI 3004295752
As of October 26, 2026, Sabormex, SAPI de C.V. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 23, 2023, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Sabormex, SAPI de C.V.
3 records, newest first. Each line links to the FDA page it came from.
2023
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2018
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2010
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Sabormex, SAPI de C.V.
- Is Sabormex, SAPI de C.V. on an FDA import alert?
- No listing for Sabormex, SAPI 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 Sabormex, SAPI de C.V.?
- No FDA import refusals for Sabormex, SAPI de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sabormex, SAPI de C.V. last inspected by FDA?
- FDA's most recent inspection of Sabormex, SAPI de C.V. with a final classification is dated March 23, 2023 and was classified NAI (No Action Indicated).
- What is Sabormex, SAPI de C.V.'s FEI number?
- Sabormex, SAPI de C.V.'s FDA Establishment Identifier (FEI) is 3004295752.
Buying from Sabormex, SAPI de C.V.?
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.