Blue Pacifico S.A.C.
FDA import alert and refusal historyTacna, PeruFEI 3009844265
As of October 26, 2026, Blue Pacifico S.A.C. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 27, 2017, most often for seafood haccp requirements not met (MFRHACCP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Fish roe, fishery products, n.e.c. · MFRHACCP
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Blue Pacifico S.A.C.
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- MFRHACCP1 refused line
Seafood HACCP requirements not met
The seafood appeared to have been processed without meeting the seafood HACCP requirements in 21 CFR 123.6(a) and 123.8(a), so it is treated as prepared under insanitary conditions.
Questions about Blue Pacifico S.A.C.
- Is Blue Pacifico S.A.C. on an FDA import alert?
- No listing for Blue Pacifico S.A.C. 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 Blue Pacifico S.A.C.?
- Yes. FDA refused 1 shipment line from Blue Pacifico S.A.C. on September 27, 2017. The most recent, on September 27, 2017, was fish roe, fishery products, n.e.c., charged as MFRHACCP (seafood haccp requirements not met).
- Why did FDA refuse Blue Pacifico S.A.C.'s shipments?
- The most frequent charge is MFRHACCP (seafood haccp requirements not met, 1 line).
- When was Blue Pacifico S.A.C. last inspected by FDA?
- FDA's most recent inspection of Blue Pacifico S.A.C. with a final classification is dated March 12, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Blue Pacifico S.A.C.'s FEI number?
- Blue Pacifico S.A.C.'s FDA Establishment Identifier (FEI) is 3009844265.
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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.