Boiron
FDA import alert and refusal historyBiot, FranceFEI 3008994794
As of October 26, 2026, Boiron is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 31, 2019, most often for directions (DIRECTIONS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · DIRECTIONS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Boiron
1 record, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.DIRECTIONSUNAPPROVEDEntry 799-3837285-9Source
Refusal charges, in plain English
- DIRECTIONS1 refused line
DIRECTIONS
- UNAPPROVED1 refused line
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Boiron
- Is Boiron on an FDA import alert?
- No listing for Boiron appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
- Has FDA refused shipments from Boiron?
- Yes. FDA refused 1 shipment line from Boiron on October 31, 2019. The most recent, on October 31, 2019, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as DIRECTIONS (directions).
- Why did FDA refuse Boiron's shipments?
- The most frequent charges are DIRECTIONS (directions, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
- What is Boiron's FEI number?
- Boiron's FDA Establishment Identifier (FEI) is 3008994794.
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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.