Ronak Exim Private Ltd.
FDA import alert and refusal historyVadodara, IndiaFEI 3012898189
As of October 26, 2026, Ronak Exim Private Ltd. (Vadodara, India) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for dr. ico cyproheptadine with multi vitamin tablets; dr. ico cyproheptadine with multivitamin tablets, published by FDA on September 18, 2025, 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 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ronak Exim Private Ltd.
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 54-16red listDR. Ico Cyproheptadine with multi vitamin tablets; DR. ICO Cyproheptadine with Multivitamin TabletsSource
Questions about Ronak Exim Private Ltd.
- Is Ronak Exim Private Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, Ronak Exim Private Ltd. is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for dr. ico cyproheptadine with multi vitamin tablets; dr. ico cyproheptadine with multivitamin tablets; FDA published the listing on September 18, 2025.
- Has FDA refused shipments from Ronak Exim Private Ltd.?
- No FDA import refusals for Ronak Exim Private Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Ronak Exim Private Ltd.'s FEI number?
- Ronak Exim Private Ltd.'s FDA Establishment Identifier (FEI) is 3012898189.
- Can shipments from Ronak Exim Private Ltd. still enter the U.S.?
- Shipments of dr. ico cyproheptadine with multi vitamin tablets; dr. ico cyproheptadine with multivitamin tablets from Ronak Exim Private Ltd. can be detained without physical examination under Import Alert 54-16; 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.