Maspex-Gmw Sp. Z O.O. Sp.K.
FDA import alert and refusal historyWadowice, PolandFEI 3002860609
Recorded by FDA as MASPEX-GMW SP. Z O.O. SP.K.
As of October 26, 2026, Maspex-Gmw Sp. Z O.O. Sp.K. (Wadowice, Poland) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for orange juice, published by FDA on June 7, 2012, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Maspex-Gmw Sp. Z O.O. Sp.K.
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2012
- Import alert listingListed on Import Alert 99-08red listOrange JuiceSource
Questions about Maspex-Gmw Sp. Z O.O. Sp.K.
- Is Maspex-Gmw Sp. Z O.O. Sp.K. on an FDA import alert?
- Yes. As of October 26, 2026, Maspex-Gmw Sp. Z O.O. Sp.K. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for orange juice; FDA published the listing on June 7, 2012.
- Has FDA refused shipments from Maspex-Gmw Sp. Z O.O. Sp.K.?
- No FDA import refusals for Maspex-Gmw Sp. Z O.O. Sp.K. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Maspex-Gmw Sp. Z O.O. Sp.K. last inspected by FDA?
- FDA's most recent inspection of Maspex-Gmw Sp. Z O.O. Sp.K. with a final classification is dated October 21, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Maspex-Gmw Sp. Z O.O. Sp.K.'s FEI number?
- Maspex-Gmw Sp. Z O.O. Sp.K.'s FDA Establishment Identifier (FEI) is 3002860609.
- Can shipments from Maspex-Gmw Sp. Z O.O. Sp.K. still enter the U.S.?
- Shipments of orange juice from Maspex-Gmw Sp. Z O.O. Sp.K. can be detained without physical examination under Import Alert 99-08; 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.