LAMBO Laboratoria
FDA import alert and refusal historyWijnegem, BelgiumFEI 3007317205
As of October 25, 2026, LAMBO Laboratoria (Wijnegem, Belgium) is on the red list of FDA Import Alert 54-14 (Supplements from firms not meeting supplement GMP) for all dietary supplement products, published by FDA on January 9, 2023, 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 list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for LAMBO Laboratoria
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 54-14red listAll Dietary Supplement ProductsSource
2022
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and EconSource
Questions about LAMBO Laboratoria
- Is LAMBO Laboratoria on an FDA import alert?
- Yes. As of October 25, 2026, LAMBO Laboratoria is on the red list of FDA Import Alert 54-14, “Supplements from firms not meeting supplement GMP”, for all dietary supplement products; FDA published the listing on January 9, 2023.
- Has FDA refused shipments from LAMBO Laboratoria?
- No FDA import refusals for LAMBO Laboratoria appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was LAMBO Laboratoria last inspected by FDA?
- FDA's most recent inspection of LAMBO Laboratoria with a final classification is dated August 12, 2022 and was classified OAI (Official Action Indicated).
- What is LAMBO Laboratoria's FEI number?
- LAMBO Laboratoria's FDA Establishment Identifier (FEI) is 3007317205.
- Can shipments from LAMBO Laboratoria still enter the U.S.?
- Shipments of all dietary supplement products from LAMBO Laboratoria 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.