Apicola de Allende, S.A. de C.V.
FDA import alert and refusal historyAllende, MexicoFEI 3008831556
As of October 26, 2026, Apicola de Allende, S.A. de C.V. (Allende, Mexico) is on the red list of FDA Import Alert 54-14 (Supplements from firms not meeting supplement GMP) for royal jelly; royal jelly capsules; propolis liquid extract drops; propolis capsules; bee pollen; espectibron, published by FDA on April 24, 2017, is also listed on Import Alert 99-39 (red list), 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 54-14 · red listIA 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 Apicola de Allende, S.A. de C.V.
4 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2017
- Import alert listingListed on Import Alert 54-14red listRoyal Jelly; Royal Jelly Capsules; Propolis Liquid Extract Drops; Propolis Capsules; Bee Pollen; EspectiBronSource
- Import alert listingListed on Import Alert 99-39red listRoyal Jelly; Royal Jelly Capsules; Propolis Liquid Extract Drops; Propolis Capsules; Bee Pollen; EspectiBronSource
2016
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and EconSource
Questions about Apicola de Allende, S.A. de C.V.
- Is Apicola de Allende, S.A. de C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Apicola de Allende, S.A. de C.V. is on the red list of FDA Import Alert 54-14, “Supplements from firms not meeting supplement GMP”, for royal jelly; royal jelly capsules; propolis liquid extract drops; propolis capsules; bee pollen; espectibron; FDA published the listing on April 24, 2017.
- Has FDA refused shipments from Apicola de Allende, S.A. de C.V.?
- No FDA import refusals for Apicola de Allende, S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Apicola de Allende, S.A. de C.V. last inspected by FDA?
- FDA's most recent inspection of Apicola de Allende, S.A. de C.V. with a final classification is dated January 13, 2022 and was classified VAI (Voluntary Action Indicated).
- What is Apicola de Allende, S.A. de C.V.'s FEI number?
- Apicola de Allende, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3008831556.
- Can shipments from Apicola de Allende, S.A. de C.V. still enter the U.S.?
- Shipments of royal jelly; royal jelly capsules; propolis liquid extract drops; propolis capsules; bee pollen; espectibron from Apicola de Allende, S.A. de C.V. can be detained without physical examination under Import Alert 54-14; 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.