Anona GmbH
FDA import alert and refusal historyColditz, GermanyFEI 3012132627
As of October 26, 2026, Anona GmbH is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on April 24, 2023, most often for unauthorized nutrient content or health claim (HEALTH C).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Dietary conventional foods, n.e.c. · LIST INGRE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Anona GmbH
2 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2023
- Import refusalRefused, Dietary conventional foods, n.e.c.LIST INGRELACKS FIRMPLANT PARTNCONTACTNUTRIT LBLHEALTH CUNAPPROVEDEntry 9TV-1007586-9Source
Refusal charges, in plain English
- HEALTH C1 refused line
Unauthorized nutrient content or health claim
The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.
- LACKS FIRM1 refused line
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE1 refused line
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- 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.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- PLANT PART1 refused line
PLANT PART
- 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 Anona GmbH
- Is Anona GmbH on an FDA import alert?
- No listing for Anona 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 Anona GmbH?
- Yes. FDA refused 1 shipment line from Anona GmbH on April 24, 2023. The most recent, on April 24, 2023, was dietary conventional foods, n.e.c., charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Anona GmbH's shipments?
- The most frequent charges are HEALTH C (unauthorized nutrient content or health claim, 1 line) and LACKS FIRM (manufacturer name and address missing, 1 line).
- When was Anona GmbH last inspected by FDA?
- FDA's most recent inspection of Anona GmbH with a final classification is dated November 14, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Anona GmbH's FEI number?
- Anona GmbH's FDA Establishment Identifier (FEI) is 3012132627.
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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.