Dabur India Limited
FDA import alert and refusal historyAlwar, IndiaFEI 3004326814
As of October 26, 2026, Dabur India Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 23, 2024, most often for pesticide chemical residue (PESTICIDE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Herbals & botanicals (not teas), n.e.c. · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Dabur India Limited
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Dabur India Limited
- Is Dabur India Limited on an FDA import alert?
- No listing for Dabur India Limited 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 Dabur India Limited?
- Yes. FDA refused 1 shipment line from Dabur India Limited on September 23, 2024. The most recent, on September 23, 2024, was herbals & botanicals (not teas), n.e.c., charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Dabur India Limited's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- When was Dabur India Limited last inspected by FDA?
- FDA's most recent inspection of Dabur India Limited with a final classification is dated July 25, 2014 and was classified OAI (Official Action Indicated).
- What is Dabur India Limited's FEI number?
- Dabur India Limited's FDA Establishment Identifier (FEI) is 3004326814.
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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.