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Langeberg Foods (PYT) Ltd.

FDA import alert and refusal historyAshton, South AfricaFEI 3013079160

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Example subjectLangeberg Foods (PYT) Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Langeberg Foods (PYT) Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on April 14, 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 Langeberg Foods (PYT) Ltd.

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

2023

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2020

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Questions about Langeberg Foods (PYT) Ltd.

Is Langeberg Foods (PYT) Ltd. on an FDA import alert?
No listing for Langeberg Foods (PYT) Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.
Has FDA refused shipments from Langeberg Foods (PYT) Ltd.?
No FDA import refusals for Langeberg Foods (PYT) Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Langeberg Foods (PYT) Ltd. last inspected by FDA?
FDA's most recent inspection of Langeberg Foods (PYT) Ltd. with a final classification is dated April 14, 2023 and was classified VAI (Voluntary Action Indicated).
What is Langeberg Foods (PYT) Ltd.'s FEI number?
Langeberg Foods (PYT) Ltd.'s FDA Establishment Identifier (FEI) is 3013079160.

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Example subjectLangeberg Foods (PYT) Ltd 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.