Lopez Laboratory
FDA import alert and refusal historyZona 10, GuatemalaFEI 3040071003
Recorded by FDA as LOPEZ LABORATORY
As of October 26, 2026, Lopez Laboratory is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 10, 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
- Foods with supplemental nutrients added, with or without artifical sweetners · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Lopez Laboratory
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Foods with supplemental nutrients added, with or without artifical sweetnersUNAPPROVEDEntry 799-4933627-7Source
Refusal charges, in plain English
- UNAPPROVED1 refused line
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 Lopez Laboratory
- Is Lopez Laboratory on an FDA import alert?
- No listing for Lopez Laboratory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
- Has FDA refused shipments from Lopez Laboratory?
- Yes. FDA refused 1 shipment line from Lopez Laboratory on November 10, 2025. The most recent, on November 10, 2025, was foods with supplemental nutrients added, with or without artifical sweetners, charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Lopez Laboratory's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Lopez Laboratory's FEI number?
- Lopez Laboratory's FDA Establishment Identifier (FEI) is 3040071003.
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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.