Qindoa Perfect Import
FDA import alert and refusal historyQingdoa, ChinaFEI 3013409435
Recorded by FDA as QINDOA PERFECT IMPORT
As of October 26, 2026, Qindoa Perfect Import (Qingdoa, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for green raisins, published by FDA on November 17, 2017, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Raisins, dried or paste · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Qindoa Perfect Import
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 refused lines
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 Qindoa Perfect Import
- Is Qindoa Perfect Import on an FDA import alert?
- Yes. As of October 26, 2026, Qindoa Perfect Import is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for green raisins; FDA published the listing on November 17, 2017.
- Has FDA refused shipments from Qindoa Perfect Import?
- Yes. FDA refused 2 shipment lines from Qindoa Perfect Import on October 25, 2017. The most recent, on October 25, 2017, was raisins, dried or paste, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Qindoa Perfect Import's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Qindoa Perfect Import's FEI number?
- Qindoa Perfect Import's FDA Establishment Identifier (FEI) is 3013409435.
- Can shipments from Qindoa Perfect Import still enter the U.S.?
- Shipments of green raisins from Qindoa Perfect Import can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.