Wawel S.A. (Dobczyce)
FDA import alert and refusal historyDobczyce, PolandFEI 2000032439
Recorded by FDA as WAWEL S.A. (DOBCZYCE)
As of October 26, 2026, Wawel S.A. (Dobczyce) has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on September 10, 2018, was classified NAI (No Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Wawel S.A. (Dobczyce)
2 records, newest first. Each line links to the FDA page it came from.
Questions about Wawel S.A. (Dobczyce)
- Is Wawel S.A. (Dobczyce) on an FDA import alert?
- No listing for Wawel S.A. (Dobczyce) appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Poland page.
- Has FDA refused shipments from Wawel S.A. (Dobczyce)?
- No FDA import refusals for Wawel S.A. (Dobczyce) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Wawel S.A. (Dobczyce) last inspected by FDA?
- FDA's most recent inspection of Wawel S.A. (Dobczyce) with a final classification is dated September 10, 2018 and was classified NAI (No Action Indicated).
- What is Wawel S.A. (Dobczyce)'s FEI number?
- Wawel S.A. (Dobczyce)'s FDA Establishment Identifier (FEI) is 2000032439.
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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.