Erdic International
FDA import alert and refusal historyEindhoven, NetherlandsFEI 3008509474
As of October 25, 2026, Erdic International (Eindhoven, Netherlands) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for herbals & botanicals (not teas), n.e.c.; vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., published by FDA on October 2, 2015, 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 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Erdic International
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-39red listHerbals & Botanicals (not Teas), N.E.C.; Vitamin, Mineral, Proteins and Unconventional Dietary Specialities For Humans and Animals, N.E.C.Source
Questions about Erdic International
- Is Erdic International on an FDA import alert?
- Yes. As of October 25, 2026, Erdic International is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for herbals & botanicals (not teas), n.e.c.; vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.; FDA published the listing on October 2, 2015.
- Has FDA refused shipments from Erdic International?
- No FDA import refusals for Erdic International appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Erdic International's FEI number?
- Erdic International's FDA Establishment Identifier (FEI) is 3008509474.
- Can shipments from Erdic International still enter the U.S.?
- Shipments of herbals & botanicals (not teas), n.e.c.; vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. from Erdic International can be detained without physical examination under Import Alert 99-39; 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.