Teatox GmbH
FDA import alert and refusal historyBerlin, GermanyFEI 3012718605
Recorded by FDA as TEATOX GMBH
As of October 26, 2026, Teatox GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on October 14, 2016, most often for not identified as a dietary supplement (DIETARYLBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Tea, n.e.c. · DIETARYLBL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Teatox GmbH
1 record, newest first. Each line links to the FDA page it came from.
2016
- Import refusalRefused, Tea, n.e.c.DIETARYLBLNCONTACTEntry UPS-0056241-4Source
Refusal charges, in plain English
- DIETARYLBL1 refused line
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- NCONTACT1 refused line
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
Questions about Teatox GmbH
- Is Teatox GmbH on an FDA import alert?
- No listing for Teatox GmbH appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
- Has FDA refused shipments from Teatox GmbH?
- Yes. FDA refused 1 shipment line from Teatox GmbH on October 14, 2016. The most recent, on October 14, 2016, was tea, n.e.c., charged as DIETARYLBL (not identified as a dietary supplement).
- Why did FDA refuse Teatox GmbH's shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 1 line) and NCONTACT (no u.s. adverse event contact on supplement label, 1 line).
- What is Teatox GmbH's FEI number?
- Teatox GmbH's FDA Establishment Identifier (FEI) is 3012718605.
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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.