Laboratorios Shela, S.A. de C.V
FDA import alert and refusal historyCiudad De Mexico, MexicoFEI 3039113427
As of October 26, 2026, Laboratorios Shela, S.A. de C.V (Ciudad De Mexico, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for neopi plus herbal supplement tablets; neopil caps, published by FDA on November 18, 2014, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Laboratorios Shela, S.A. de C.V
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 45-02red listNeopi Plus Herbal Supplement Tablets; NEOPIL CAPSSource
Questions about Laboratorios Shela, S.A. de C.V
- Is Laboratorios Shela, S.A. de C.V on an FDA import alert?
- Yes. As of October 26, 2026, Laboratorios Shela, S.A. de C.V is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for neopi plus herbal supplement tablets; neopil caps; FDA published the listing on November 18, 2014.
- Has FDA refused shipments from Laboratorios Shela, S.A. de C.V?
- No FDA import refusals for Laboratorios Shela, S.A. de C.V appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Laboratorios Shela, S.A. de C.V's FEI number?
- Laboratorios Shela, S.A. de C.V's FDA Establishment Identifier (FEI) is 3039113427.
- Can shipments from Laboratorios Shela, S.A. de C.V still enter the U.S.?
- Shipments of neopi plus herbal supplement tablets; neopil caps from Laboratorios Shela, S.A. de C.V can be detained without physical examination under Import Alert 45-02; 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.