Omnilife Manufactura S.A. de C.V.
FDA import alert and refusal historyTlaquepaque, MexicoFEI 3004266321
As of October 26, 2026, Omnilife Manufactura S.A. de C.V. is on the green list of FDA Import Alert 21-07, which exempts its listed products from detention without physical examination under that alert, 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 21-07 · green list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Omnilife Manufactura S.A. de C.V.
4 records, newest first. Each line links to the FDA page it came from.
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and EconSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and EconSource
2009
- Import alert listingListed on Import Alert 21-07green listEgo Thermogen Cola with Tamarind ExtractSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Omnilife Manufactura S.A. de C.V.
- Is Omnilife Manufactura S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Omnilife Manufactura S.A. de C.V. is on the green list of FDA Import Alert 21-07, “Tamarind and tamarind products: filth”, for ego thermogen cola with tamarind extract; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Omnilife Manufactura S.A. de C.V.?
- No FDA import refusals for Omnilife Manufactura S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Omnilife Manufactura S.A. de C.V. last inspected by FDA?
- FDA's most recent inspection of Omnilife Manufactura S.A. de C.V. with a final classification is dated December 6, 2018 and was classified VAI (Voluntary Action Indicated).
- What is Omnilife Manufactura S.A. de C.V.'s FEI number?
- Omnilife Manufactura S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3004266321.
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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.