Calimenta - Agroindustria, S.A.
FDA import alert and refusal historyCaldas Da Rainha, PortugalFEI 3013607730
As of October 27, 2026, Calimenta - Agroindustria, S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 3, 2018, most often for no scheduled process filed (NO PROCESS).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Pepper sauce (hot, mild, etc.) · NO PROCESS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Calimenta - Agroindustria, S.A.
1 record, newest first. Each line links to the FDA page it came from.
2018
- Import refusalRefused, Pepper sauce (hot, mild, etc.)NO PROCESSEntry 334-5804519-3Source
Refusal charges, in plain English
- NO PROCESS1 refused line
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
Questions about Calimenta - Agroindustria, S.A.
- Is Calimenta - Agroindustria, S.A. on an FDA import alert?
- No listing for Calimenta - Agroindustria, S.A. appears in the FDA import alerts SupplierRadar checked on October 27, 2026. Country-wide alerts may still apply to its products; see the Portugal page.
- Has FDA refused shipments from Calimenta - Agroindustria, S.A.?
- Yes. FDA refused 1 shipment line from Calimenta - Agroindustria, S.A. on July 3, 2018. The most recent, on July 3, 2018, was pepper sauce (hot, mild, etc.), charged as NO PROCESS (no scheduled process filed).
- Why did FDA refuse Calimenta - Agroindustria, S.A.'s shipments?
- The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
- What is Calimenta - Agroindustria, S.A.'s FEI number?
- Calimenta - Agroindustria, S.A.'s FDA Establishment Identifier (FEI) is 3013607730.
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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.