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IQF del Peru S.A. (Chincha factory)

FDA import alert and refusal historyChincha, PeruFEI 3004276095

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Example subjectIQF del Peru S.A. (Chincha factory added to Import Alert 16-129 (red list)

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As of October 26, 2026, IQF del Peru S.A. (Chincha factory) has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 8, 2016, 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 IQF del Peru S.A. (Chincha factory)

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

2016

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2011

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Questions about IQF del Peru S.A. (Chincha factory)

Is IQF del Peru S.A. (Chincha factory) on an FDA import alert?
No listing for IQF del Peru S.A. (Chincha factory) 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 IQF del Peru S.A. (Chincha factory)?
No FDA import refusals for IQF del Peru S.A. (Chincha factory) appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was IQF del Peru S.A. (Chincha factory) last inspected by FDA?
FDA's most recent inspection of IQF del Peru S.A. (Chincha factory) with a final classification is dated March 8, 2016 and was classified NAI (No Action Indicated).
What is IQF del Peru S.A. (Chincha factory)'s FEI number?
IQF del Peru S.A. (Chincha factory)'s FDA Establishment Identifier (FEI) is 3004276095.

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Example subjectIQF del Peru S.A. (Chincha factory 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.