Crisosa, S.A. de C.V.
FDA import alert and refusal historyTijuana, MexicoFEI 3013616348
Recorded by FDA as CRISOSA, S.A. DE C.V.
As of October 26, 2026, Crisosa, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 7, 2017, most often for artificial coloring not declared (COLOR LBLG).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Gelatin, n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Crisosa, S.A. de C.V.
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Gelatin, n.e.c.UNSAFE COLCOLOR LBLGEntry 9L9-0134324-9Source
Refusal charges, in plain English
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Crisosa, S.A. de C.V.
- Is Crisosa, S.A. de C.V. on an FDA import alert?
- No listing for Crisosa, S.A. de C.V. 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 Crisosa, S.A. de C.V.?
- Yes. FDA refused 1 shipment line from Crisosa, S.A. de C.V. on September 7, 2017. The most recent, on September 7, 2017, was gelatin, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Crisosa, S.A. de C.V.'s shipments?
- The most frequent charges are COLOR LBLG (artificial coloring not declared, 1 line) and UNSAFE COL (color additive unsafe under section 721, 1 line).
- What is Crisosa, S.A. de C.V.'s FEI number?
- Crisosa, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3013616348.
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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.