La Piedra Redonda S.L. (Consorcio Exportador Andaluz)
FDA import alert and refusal historyZamoranos, SpainFEI 3009928065
As of October 26, 2026, La Piedra Redonda S.L. (Consorcio Exportador Andaluz) has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 5, 2023, was classified VAI (Voluntary 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 VAI (Voluntary Action Indicated)
Every FDA record for La Piedra Redonda S.L. (Consorcio Exportador Andaluz)
2 records, newest first. Each line links to the FDA page it came from.
Questions about La Piedra Redonda S.L. (Consorcio Exportador Andaluz)
- Is La Piedra Redonda S.L. (Consorcio Exportador Andaluz) on an FDA import alert?
- No listing for La Piedra Redonda S.L. (Consorcio Exportador Andaluz) appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
- Has FDA refused shipments from La Piedra Redonda S.L. (Consorcio Exportador Andaluz)?
- No FDA import refusals for La Piedra Redonda S.L. (Consorcio Exportador Andaluz) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was La Piedra Redonda S.L. (Consorcio Exportador Andaluz) last inspected by FDA?
- FDA's most recent inspection of La Piedra Redonda S.L. (Consorcio Exportador Andaluz) with a final classification is dated May 5, 2023 and was classified VAI (Voluntary Action Indicated).
- What is La Piedra Redonda S.L. (Consorcio Exportador Andaluz)'s FEI number?
- La Piedra Redonda S.L. (Consorcio Exportador Andaluz)'s FDA Establishment Identifier (FEI) is 3009928065.
Buying from La Piedra Redonda S.L. (Consorcio Exportador Andaluz)?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.