A-ware Packaging B.V.
FDA import alert and refusal historyZeewolde, NetherlandsFEI 3004386909
As of October 25, 2026, A-ware Packaging B.V. (Zeewolde, Netherlands) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for maasdam cheese, published by FDA on March 28, 2022, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-45 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for A-ware Packaging B.V.
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-45red listMaasdam CheeseSource
2013
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about A-ware Packaging B.V.
- Is A-ware Packaging B.V. on an FDA import alert?
- Yes. As of October 25, 2026, A-ware Packaging B.V. is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for maasdam cheese; FDA published the listing on March 28, 2022.
- Has FDA refused shipments from A-ware Packaging B.V.?
- No FDA import refusals for A-ware Packaging B.V. appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was A-ware Packaging B.V. last inspected by FDA?
- FDA's most recent inspection of A-ware Packaging B.V. with a final classification is dated August 29, 2013 and was classified OAI (Official Action Indicated).
- What is A-ware Packaging B.V.'s FEI number?
- A-ware Packaging B.V.'s FDA Establishment Identifier (FEI) is 3004386909.
- Can shipments from A-ware Packaging B.V. still enter the U.S.?
- Shipments of maasdam cheese from A-ware Packaging B.V. can be detained without physical examination under Import Alert 99-45; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.