Gialive SA de CV
FDA import alert and refusal historyAguascalientes, MexicoFEI 3010203534
As of October 26, 2026, Gialive SA de CV (Aguascalientes, Mexico) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for gia lactium f, published by FDA on October 2, 2015, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Gialive SA de CV
3 records, newest first. Each line links to the FDA page it came from.
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and EconSource
2015
- Import alert listingListed on Import Alert 99-39red listGIA Lactium FSource
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and EconSource
Questions about Gialive SA de CV
- Is Gialive SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Gialive SA de CV is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for gia lactium f; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Gialive SA de CV?
- No FDA import refusals for Gialive SA de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Gialive SA de CV last inspected by FDA?
- FDA's most recent inspection of Gialive SA de CV with a final classification is dated December 7, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Gialive SA de CV's FEI number?
- Gialive SA de CV's FDA Establishment Identifier (FEI) is 3010203534.
- Can shipments from Gialive SA de CV still enter the U.S.?
- Shipments of gia lactium f from Gialive SA de CV can be detained without physical examination under Import Alert 99-39; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.