K.P. Enterprise
FDA import alert and refusal historyDhrangadhra, IndiaFEI 3006501661
Recorded by FDA as K.P. ENTERPRISE
As of October 26, 2026, K.P. Enterprise is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on June 6, 2025, most often for fair packaging and labeling act (LABELING).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tzahp choy (chinese canned sweet pickles made from mixed vegetables), with sauce · LABELING
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for K.P. Enterprise
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: Tzahp choy (chinese canned sweet pickles made from mixed vegetables), with sauceLABELINGEntry KM6-3650967-1Show 2 linesHide lines
Refusal charges, in plain English
- LABELING2 refused lines
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 K.P. Enterprise
- Is K.P. Enterprise on an FDA import alert?
- No listing for K.P. Enterprise 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 K.P. Enterprise?
- Yes. FDA refused 2 shipment lines from K.P. Enterprise on June 6, 2025. The most recent, on June 6, 2025, was tzahp choy (chinese canned sweet pickles made from mixed vegetables), with sauce, charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse K.P. Enterprise's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 2 lines).
- What is K.P. Enterprise's FEI number?
- K.P. Enterprise's FDA Establishment Identifier (FEI) is 3006501661.
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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.