Sydenham Laboratorio
FDA import alert and refusal historyPuebla, MexicoFEI 3020052365
Recorded by FDA as SYDENHAM LABORATORIO
As of October 25, 2026, Sydenham Laboratorio is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between May 16, 2025 and May 28, 2025, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Folic acid (vitamin) · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Sydenham Laboratorio
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Folic acid (vitamin)UNAPPROVEDEntry 799-7537855-6Source
- Import refusalRefused, Folic acid (vitamin)UNAPPROVEDEntry 799-7679341-5Source
Refusal charges, in plain English
- UNAPPROVED2 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Sydenham Laboratorio
- Is Sydenham Laboratorio on an FDA import alert?
- No listing for Sydenham Laboratorio appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Sydenham Laboratorio?
- Yes. FDA refused 2 shipment lines from Sydenham Laboratorio between May 16, 2025 and May 28, 2025. The most recent, on May 28, 2025, was folic acid (vitamin), charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Sydenham Laboratorio's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Sydenham Laboratorio's FEI number?
- Sydenham Laboratorio's FDA Establishment Identifier (FEI) is 3020052365.
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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.