Camaronera la Gloria Marina, S.A.
FDA import alert and refusal historyVilla Nueva, GuatemalaFEI 3021659733
Recorded by FDA as CAMARONERA LA GLORIA MARINA, S.A.
As of October 26, 2026, Camaronera la Gloria Marina, S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 7, 2022, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Mackerel (all except scomberomorus sp, eg spanish or king see '22') · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Camaronera la Gloria Marina, S.A.
1 record, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Camaronera la Gloria Marina, S.A.
- Is Camaronera la Gloria Marina, S.A. on an FDA import alert?
- No listing for Camaronera la Gloria Marina, 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 Guatemala page.
- Has FDA refused shipments from Camaronera la Gloria Marina, S.A.?
- Yes. FDA refused 1 shipment line from Camaronera la Gloria Marina, S.A. on April 7, 2022. The most recent, on April 7, 2022, was mackerel (all except scomberomorus sp, eg spanish or king see '22'), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Camaronera la Gloria Marina, S.A.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- What is Camaronera la Gloria Marina, S.A.'s FEI number?
- Camaronera la Gloria Marina, S.A.'s FDA Establishment Identifier (FEI) is 3021659733.
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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.