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Inversiones Peru Pacifico S.A.

FDA import alert and refusal historyCallao, PeruFEI 3010142288

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Example subjectInversiones Peru Pacifico S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Inversiones Peru Pacifico S.A. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 20, 2017, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)

Every FDA record for Inversiones Peru Pacifico S.A.

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

2017

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

2014

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

Questions about Inversiones Peru Pacifico S.A.

Is Inversiones Peru Pacifico S.A. on an FDA import alert?
No listing for Inversiones Peru Pacifico S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Peru page.
Has FDA refused shipments from Inversiones Peru Pacifico S.A.?
No FDA import refusals for Inversiones Peru Pacifico S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Inversiones Peru Pacifico S.A. last inspected by FDA?
FDA's most recent inspection of Inversiones Peru Pacifico S.A. with a final classification is dated September 20, 2017 and was classified VAI (Voluntary Action Indicated).
What is Inversiones Peru Pacifico S.A.'s FEI number?
Inversiones Peru Pacifico S.A.'s FDA Establishment Identifier (FEI) is 3010142288.

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Example subjectInversiones Peru Pacifico S.A 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.