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Serramonte Enterprise

FDA import alert and refusal historySan Juan, PhilippinesFEI 3003837581

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Example subjectSerramonte Enterpris added to Import Alert 16-129 (red list)

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As of October 25, 2026, Serramonte Enterprise has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on December 2, 2019, was classified NAI (No Action Indicated).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Serramonte Enterprise

3 records, newest first. Each line links to the FDA page it came from.

2019

  1. Inspection
    Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2016

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2011

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Questions about Serramonte Enterprise

Is Serramonte Enterprise on an FDA import alert?
No listing for Serramonte Enterprise appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Philippines page.
Has FDA refused shipments from Serramonte Enterprise?
No FDA import refusals for Serramonte Enterprise appear in FDA's refusal data since October 2016, as of October 25, 2026.
When was Serramonte Enterprise last inspected by FDA?
FDA's most recent inspection of Serramonte Enterprise with a final classification is dated December 2, 2019 and was classified NAI (No Action Indicated).
What is Serramonte Enterprise's FEI number?
Serramonte Enterprise's FDA Establishment Identifier (FEI) is 3003837581.

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Example subjectSerramonte Enterpris added to Import Alert 16-129 (red list)

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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.