Laboratoires Quinton Internation
FDA import alert and refusal historyAlicante, SpainFEI 3041727736
Recorded by FDA as LABORATOIRES QUINTON INTERNATION
As of October 26, 2026, Laboratoires Quinton Internation is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 22, 2026, most often for no u.s. adverse event contact on supplement label (NCONTACT).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NCONTACT
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Laboratoires Quinton Internation
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACTNUTRIT LBLEntry 1FX-3065020-5Source
Refusal charges, in plain English
- NCONTACT1 refused line
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about Laboratoires Quinton Internation
- Is Laboratoires Quinton Internation on an FDA import alert?
- No listing for Laboratoires Quinton Internation appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
- Has FDA refused shipments from Laboratoires Quinton Internation?
- Yes. FDA refused 1 shipment line from Laboratoires Quinton Internation on September 22, 2026. The most recent, on September 22, 2026, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).
- Why did FDA refuse Laboratoires Quinton Internation's shipments?
- The most frequent charges are NCONTACT (no u.s. adverse event contact on supplement label, 1 line) and NUTRIT LBL (nutrition information missing from label, 1 line).
- What is Laboratoires Quinton Internation's FEI number?
- Laboratoires Quinton Internation's FDA Establishment Identifier (FEI) is 3041727736.
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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.