Abbott Laboratories S.A.
FDA import alert and refusal historyGranada, SpainFEI 3010211251
As of October 26, 2026, Abbott Laboratories S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 26, 2017, most often for nutrition information missing from label (NUTRIT LBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Foods with supplemental nutrients added, with or without artifical sweetners · NUTRIT LBL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Abbott Laboratories S.A.
1 record, newest first. Each line links to the FDA page it came from.
2017
- Import refusalRefused, Foods with supplemental nutrients added, with or without artifical sweetnersNUTRIT LBLEntry AEK-3504803-9Source
Refusal charges, in plain English
- 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 Abbott Laboratories S.A.
- Is Abbott Laboratories S.A. on an FDA import alert?
- No listing for Abbott Laboratories S.A. 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 Abbott Laboratories S.A.?
- Yes. FDA refused 1 shipment line from Abbott Laboratories S.A. on June 26, 2017. The most recent, on June 26, 2017, was foods with supplemental nutrients added, with or without artifical sweetners, charged as NUTRIT LBL (nutrition information missing from label).
- Why did FDA refuse Abbott Laboratories S.A.'s shipments?
- The most frequent charge is NUTRIT LBL (nutrition information missing from label, 1 line).
- What is Abbott Laboratories S.A.'s FEI number?
- Abbott Laboratories S.A.'s FDA Establishment Identifier (FEI) is 3010211251.
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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.