Nadh GmbH
FDA import alert and refusal historyVienna, AustriaFEI 3037120701
Recorded by FDA as NADH GMBH
As of October 27, 2026, Nadh GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 19, 2025, most often for product not listed with fda (NOT LISTED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Nicotinamide (niacinamide) (vitamin) · NOT LISTED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Nadh GmbH
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Nicotinamide (niacinamide) (vitamin)NOT LISTEDUNAPPROVEDEntry 799-7420005-8Source
Refusal charges, in plain English
- NOT LISTED1 refused line
Product not listed with FDA
The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.
- 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 Nadh GmbH
- Is Nadh GmbH on an FDA import alert?
- No listing for Nadh GmbH appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Austria page.
- Has FDA refused shipments from Nadh GmbH?
- Yes. FDA refused 1 shipment line from Nadh GmbH on May 19, 2025. The most recent, on May 19, 2025, was nicotinamide (niacinamide) (vitamin), charged as NOT LISTED (product not listed with fda).
- Why did FDA refuse Nadh GmbH's shipments?
- The most frequent charges are NOT LISTED (product not listed with fda, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
- What is Nadh GmbH's FEI number?
- Nadh GmbH's FDA Establishment Identifier (FEI) is 3037120701.
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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.