Angaga Market SA de CV
FDA import alert and refusal historyHermosillo, MexicoFEI 3012753461
Recorded by FDA as ANGAGA MARKET SA DE CV
As of October 26, 2026, Angaga Market SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 23, 2016, most often for false or misleading labeling (FALSE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Oral rehydration products · STD QUALIT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Angaga Market SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import refusalSource
Refused, 2 lines in one entry: Oral rehydration productsSTD QUALITFALSEEntry 264-0583751-4Show 2 linesHide lines
- Refused, Oral rehydration productsSTD QUALITFALSEEntry 264-0583751-4Source
- Refused, Oral rehydration productsSTD QUALITFALSEEntry 264-0583751-4Source
Refusal charges, in plain English
- FALSE2 refused lines
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- STD QUALIT2 refused lines
STD QUALIT
Questions about Angaga Market SA de CV
- Is Angaga Market SA de CV on an FDA import alert?
- No listing for Angaga Market SA de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Angaga Market SA de CV?
- Yes. FDA refused 2 shipment lines from Angaga Market SA de CV on November 23, 2016. The most recent, on November 23, 2016, was oral rehydration products, charged as STD QUALIT (std qualit).
- Why did FDA refuse Angaga Market SA de CV's shipments?
- The most frequent charges are FALSE (false or misleading labeling, 2 lines) and STD QUALIT (std qualit, 2 lines).
- What is Angaga Market SA de CV's FEI number?
- Angaga Market SA de CV's FDA Establishment Identifier (FEI) is 3012753461.
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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.