Vinodhini M C O
FDA import alert and refusal historyVellore, IndiaFEI 3044715116
Recorded by FDA as VINODHINI M C O
As of October 26, 2026, Vinodhini M C O is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 16, 2026, 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
- Candy specialties, n.e.c. (without chocolate) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Vinodhini M C O
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.
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about Vinodhini M C O
- Is Vinodhini M C O on an FDA import alert?
- No listing for Vinodhini M C O appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Vinodhini M C O?
- Yes. FDA refused 1 shipment line from Vinodhini M C O on June 16, 2026. The most recent, on June 16, 2026, was candy specialties, n.e.c. (without chocolate), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Vinodhini M C O's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 1 line) and LABELING (fair packaging and labeling act, 1 line).
- What is Vinodhini M C O's FEI number?
- Vinodhini M C O's FDA Establishment Identifier (FEI) is 3044715116.
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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.