Bahia Mares del Pacifico SAS
FDA import alert and refusal historyBuenaventura, ColombiaFEI 3029978209
Recorded by FDA as BAHIA MARES DEL PACIFICO SAS
As of October 26, 2026, Bahia Mares del Pacifico SAS is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines on October 9, 2024, most often for std qualit (STD QUALIT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Crab · STD QUALIT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Bahia Mares del Pacifico SAS
6 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 6 lines in one entry: CrabSTD QUALITEntry AMN-0097566-0Show 6 linesHide lines
- Refused, CrabSTD QUALITEntry AMN-0097566-0Source
- Refused, CrabSTD QUALITEntry AMN-0097566-0Source
- Refused, CrabSTD QUALITEntry AMN-0097566-0Source
- Refused, CrabSTD QUALITEntry AMN-0097566-0Source
- Refused, CrabSTD QUALITEntry AMN-0097566-0Source
- Refused, CrabSTD QUALITEntry AMN-0097566-0Source
Refusal charges, in plain English
- STD QUALIT6 refused lines
STD QUALIT
Questions about Bahia Mares del Pacifico SAS
- Is Bahia Mares del Pacifico SAS on an FDA import alert?
- No listing for Bahia Mares del Pacifico SAS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
- Has FDA refused shipments from Bahia Mares del Pacifico SAS?
- Yes. FDA refused 6 shipment lines from Bahia Mares del Pacifico SAS on October 9, 2024. The most recent, on October 9, 2024, was crab, charged as STD QUALIT (std qualit).
- Why did FDA refuse Bahia Mares del Pacifico SAS's shipments?
- The most frequent charge is STD QUALIT (std qualit, 6 lines).
- What is Bahia Mares del Pacifico SAS's FEI number?
- Bahia Mares del Pacifico SAS's FDA Establishment Identifier (FEI) is 3029978209.
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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.