SupplierRadar

Aqualande SAS

FDA import alert and refusal historyRoquefort, FranceFEI 3004982146

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Example subjectAqualande SA added to Import Alert 16-129 (red list)

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As of October 25, 2026, Aqualande SAS is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on February 1, 2017, most often for manufacturer name and address missing (LACKS FIRM).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Fish roe, fishery products, n.e.c. · LACKS FIRM
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Aqualande SAS

5 records, newest first. Each line links to the FDA page it came from.

2017

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source
  2. Import refusal
    Refused, Fish roe, fishery products, n.e.c.LACKS FIRMLACKS N/CUSUAL NAMENUTRIT LBLNO PROCESSEntry WBA-9159651-9
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Fish roe, fishery products, n.e.c.LACKS FIRMLACKS N/CUSUAL NAMENUTRIT LBLEntry WBA-9159423-3Show 2 lines
    Source
  4. Import refusal
    Refused, Fish roe, fishery products, n.e.c.LACKS FIRMLACKS N/CUSUAL NAMENUTRIT LBLNO PROCESSEntry WBA-9159651-9
    Source

Refusal charges, in plain English

  • LACKS FIRM4 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • LACKS N/C4 refused lines

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • NO PROCESS4 refused lines

    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.

  • NUTRIT LBL4 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • USUAL NAME4 refused lines

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

Questions about Aqualande SAS

Is Aqualande SAS on an FDA import alert?
No listing for Aqualande SAS appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Aqualande SAS?
Yes. FDA refused 4 shipment lines from Aqualande SAS on February 1, 2017. The most recent, on February 1, 2017, was fish roe, fishery products, n.e.c., charged as LACKS FIRM (manufacturer name and address missing).
Why did FDA refuse Aqualande SAS's shipments?
The most frequent charges are LACKS FIRM (manufacturer name and address missing, 4 lines) and LACKS N/C (net quantity statement missing, 4 lines).
When was Aqualande SAS last inspected by FDA?
FDA's most recent inspection of Aqualande SAS with a final classification is dated December 7, 2017 and was classified VAI (Voluntary Action Indicated).
What is Aqualande SAS's FEI number?
Aqualande SAS's FDA Establishment Identifier (FEI) is 3004982146.

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Example subjectAqualande SA added to Import Alert 16-129 (red list)

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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.