Manuela Lopez Pedro
FDA import alert and refusal historyHuehuetenango, GuatemalaFEI 3039161071
Recorded by FDA as MANUELA LOPEZ PEDRO
As of October 26, 2026, Manuela Lopez Pedro is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 24, 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
- Spices, flavors and salt not mentioned elsewhere, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Manuela Lopez Pedro
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Spices, flavors and salt not mentioned elsewhere, n.e.c.UNAPPROVEDEntry 799-1074891-4Source
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 Manuela Lopez Pedro
- Is Manuela Lopez Pedro on an FDA import alert?
- No listing for Manuela Lopez Pedro 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 Manuela Lopez Pedro?
- Yes. FDA refused 1 shipment line from Manuela Lopez Pedro on September 24, 2025. The most recent, on September 24, 2025, was spices, flavors and salt not mentioned elsewhere, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Manuela Lopez Pedro's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
- What is Manuela Lopez Pedro's FEI number?
- Manuela Lopez Pedro's FDA Establishment Identifier (FEI) is 3039161071.
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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.