Amol Biotech Limited
FDA import alert and refusal historyShanghai, ChinaFEI 3005156292
As of October 26, 2026, Amol Biotech Limited (Shanghai, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for ginseng extract powder, published by FDA on September 16, 2009, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Amol Biotech Limited
3 records, newest first. Each line links to the FDA page it came from.
2017
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2012
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and EconSource
2009
- Import alert listingListed on Import Alert 99-08red listGinseng Extract PowderSource
Questions about Amol Biotech Limited
- Is Amol Biotech Limited on an FDA import alert?
- Yes. As of October 26, 2026, Amol Biotech Limited is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for ginseng extract powder; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Amol Biotech Limited?
- No FDA import refusals for Amol Biotech Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Amol Biotech Limited last inspected by FDA?
- FDA's most recent inspection of Amol Biotech Limited with a final classification is dated December 13, 2017 and was classified NAI (No Action Indicated).
- What is Amol Biotech Limited's FEI number?
- Amol Biotech Limited's FDA Establishment Identifier (FEI) is 3005156292.
- Can shipments from Amol Biotech Limited still enter the U.S.?
- Shipments of ginseng extract powder from Amol Biotech Limited 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.