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Influx Healthcare

FDA import alert and refusal historyThane, IndiaFEI 3015150360

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As of October 26, 2026, Influx Healthcare is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between August 21, 2026 and September 25, 2026, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Biotin (vitamin h, coenzyme r) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Influx Healthcare

2 records, newest first. Each line links to the FDA page it came from.

2026

  1. Import refusal
    Refused, Biotin (vitamin h, coenzyme r)UNAPPROVEDEntry 1FX-5695390-5
    Source
  2. Import refusal
    Refused, Vitamin, n.e.c.UNAPPROVEDEntry 1FX-8484185-7
    Source

Refusal charges, in plain English

  • UNAPPROVED2 refused lines

    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 Influx Healthcare

Is Influx Healthcare on an FDA import alert?
No listing for Influx Healthcare appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
Has FDA refused shipments from Influx Healthcare?
Yes. FDA refused 2 shipment lines from Influx Healthcare between August 21, 2026 and September 25, 2026. The most recent, on September 25, 2026, was biotin (vitamin h, coenzyme r), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Influx Healthcare's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Influx Healthcare's FEI number?
Influx Healthcare's FDA Establishment Identifier (FEI) is 3015150360.

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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.