M/S. Shah Amrutlal Bachubhai & Company
FDA import alert and refusal historyMumbai, IndiaFEI 3006109995
Recorded by FDA as M/S. SHAH AMRUTLAL BACHUBHAI & COMPANY
As of October 26, 2026, M/S. Shah Amrutlal Bachubhai & Company (Mumbai, India) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for turmeric, whole (spice); turmeric, ground, cracked (spice), 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for M/S. Shah Amrutlal Bachubhai & Company
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-19red listTurmeric, Whole (Spice); Turmeric, Ground, Cracked (Spice)Source
Questions about M/S. Shah Amrutlal Bachubhai & Company
- Is M/S. Shah Amrutlal Bachubhai & Company on an FDA import alert?
- Yes. As of October 26, 2026, M/S. Shah Amrutlal Bachubhai & Company is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for turmeric, whole (spice); turmeric, ground, cracked (spice); FDA published the listing on September 16, 2009.
- Has FDA refused shipments from M/S. Shah Amrutlal Bachubhai & Company?
- No FDA import refusals for M/S. Shah Amrutlal Bachubhai & Company appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is M/S. Shah Amrutlal Bachubhai & Company's FEI number?
- M/S. Shah Amrutlal Bachubhai & Company's FDA Establishment Identifier (FEI) is 3006109995.
- Can shipments from M/S. Shah Amrutlal Bachubhai & Company still enter the U.S.?
- Shipments of turmeric, whole (spice); turmeric, ground, cracked (spice) from M/S. Shah Amrutlal Bachubhai & Company can be detained without physical examination under Import Alert 99-19; 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.